Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 15 59323779 59323779 + Missense_Mutation SNP C C G TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr15:59323779C>G c.758C>G c.(757-759)tCt>tGt p.S253C BLCA 15 59323899 59323899 + Nonsense_Mutation SNP C C G TCGA-K4-A6MB-01A-11D-A31L-08 TCGA-K4-A6MB-10A-01D-A31J-08 g.chr15:59323899C>G c.878C>G c.(877-879)tCa>tGa p.S293* BLCA 15 59344515 59344515 + Missense_Mutation SNP G G A TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr15:59344515G>A c.892G>A c.(892-894)Gaa>Aaa p.E298K BLCA 15 59348035 59348035 + Missense_Mutation SNP G G A TCGA-K4-A6MB-01A-11D-A31L-08 TCGA-K4-A6MB-10A-01D-A31J-08 g.chr15:59348035G>A c.1162G>A c.(1162-1164)Gat>Aat p.D388N BLCA 15 59350651 59350651 + Missense_Mutation SNP C C T TCGA-G2-A2EF-01A-12D-A18F-08 TCGA-G2-A2EF-10A-01D-A18F-08 g.chr15:59350651C>T c.1268C>T c.(1267-1269)tCt>tTt p.S423F BLCA 15 59350705 59350705 + Missense_Mutation SNP C C T TCGA-G2-A2EF-01A-12D-A18F-08 TCGA-G2-A2EF-10A-01D-A18F-08 g.chr15:59350705C>T c.1322C>T c.(1321-1323)tCa>tTa p.S441L BLCA 15 59350741 59350741 + Missense_Mutation SNP C C G TCGA-G2-A2EF-01A-12D-A18F-08 TCGA-G2-A2EF-10A-01D-A18F-08 g.chr15:59350741C>G c.1358C>G c.(1357-1359)tCt>tGt p.S453C BLCA 15 59358969 59358969 + Nonsense_Mutation SNP C C G TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr15:59358969C>G c.1373C>G c.(1372-1374)tCa>tGa p.S458* BLCA 15 59368241 59368241 + Missense_Mutation SNP G G A TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr15:59368241G>A c.1775G>A c.(1774-1776)tGc>tAc p.C592Y BLCA 15 59368279 59368279 + Nonsense_Mutation SNP C C T TCGA-UY-A78L-01A-12D-A339-08 TCGA-UY-A78L-10A-01D-A339-08 g.chr15:59368279C>T c.1813C>T c.(1813-1815)Cag>Tag p.Q605* BLCA 15 59373153 59373153 + Missense_Mutation SNP C C G TCGA-XF-A9SZ-01A-11D-A391-08 TCGA-XF-A9SZ-10A-01D-A394-08 g.chr15:59373153C>G c.1967C>G c.(1966-1968)cCa>cGa p.P656R BLCA 15 59373161 59373161 + Missense_Mutation SNP C C T TCGA-FD-A62P-01A-32D-A30E-08 TCGA-FD-A62P-10A-01D-A30H-08 g.chr15:59373161C>T c.1975C>T c.(1975-1977)Cat>Tat p.H659Y BLCA 15 59376398 59376398 + Missense_Mutation SNP C C T TCGA-KQ-A41O-01A-12D-A34U-08 TCGA-KQ-A41O-10D-01D-A34X-08 g.chr15:59376398C>T c.2368C>T c.(2368-2370)Cat>Tat p.H790Y BLCA 15 59376407 59376407 + Nonsense_Mutation SNP C C T TCGA-KQ-A41O-01A-12D-A34U-08 TCGA-KQ-A41O-10D-01D-A34X-08 g.chr15:59376407C>T c.2377C>T c.(2377-2379)Cag>Tag p.Q793* BLCA 15 59377984 59377984 + Splice_Site SNP G G C TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr15:59377984G>C c.2550G>C c.(2548-2550)atG>atC p.M850I BLCA 15 59381909 59381909 + Nonsense_Mutation SNP C C G TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr15:59381909C>G c.2594C>G c.(2593-2595)tCa>tGa p.S865* BLCA 15 59381927 59381927 + Missense_Mutation SNP C C T TCGA-XF-AAN2-01A-11D-A42E-08 TCGA-XF-AAN2-10A-01D-A42H-08 g.chr15:59381927C>T c.2612C>T c.(2611-2613)tCa>tTa p.S871L BLCA 15 59384757 59384757 + Missense_Mutation SNP G G C TCGA-GU-A767-01A-11D-A32B-08 TCGA-GU-A767-10A-01D-A329-08 g.chr15:59384757G>C c.2785G>C c.(2785-2787)Gat>Cat p.D929H BRCA 15 59323149 59323149 + Missense_Mutation SNP T T A TCGA-E9-A243-01A-21D-A167-09 TCGA-E9-A243-10A-01D-A17G-09 g.chr15:59323149T>A c.128T>A c.(127-129)aTt>aAt p.I43N BRCA 15 59323732 59323732 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr15:59323732G>T c.711G>T c.(709-711)aaG>aaT p.K237N BRCA 15 59347900 59347900 + Missense_Mutation SNP C C T TCGA-AC-A2BK-01A-11D-A21Q-09 TCGA-AC-A2BK-11A-13D-A21Q-09 g.chr15:59347900C>T c.1027C>T c.(1027-1029)Cac>Tac p.H343Y BRCA 15 59350671 59350671 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr15:59350671A>C c.1288A>C c.(1288-1290)Acc>Ccc p.T430P BRCA 15 59359165 59359165 + Frame_Shift_Del DEL C C - TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr15:59359165delC c.1569delC c.(1567-1569)cacfs p.H523fs BRCA 15 59368259 59368259 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr15:59368259G>A c.1793G>A c.(1792-1794)cGa>cAa p.R598Q BRCA 15 59368377 59368380 + Frame_Shift_Del DEL CTCT CTCT - TCGA-AO-A0J3-01A-11W-A050-09 TCGA-AO-A0J3-10A-01W-A055-09 g.chr15:59368377_59368380delCTCT c.1911_1914delCTCT c.(1909-1914)ccctctfs p.PS637fs BRCA 15 59373484 59373484 + Splice_Site SNP G G A TCGA-LQ-A4E4-01A-11D-A25Q-09 TCGA-LQ-A4E4-10A-01D-A25Q-09 g.chr15:59373484G>A c.e8+1 BRCA 15 59377902 59377902 + Missense_Mutation SNP C C T TCGA-E9-A3HO-01A-11D-A20S-09 TCGA-E9-A3HO-10A-02D-A20S-09 g.chr15:59377902C>T c.2468C>T c.(2467-2469)cCt>cTt p.P823L BRCA 15 59384805 59384808 + Frame_Shift_Del DEL TGTT TGTT - TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr15:59384805_59384808delTGTT c.2833_2836delTGTT c.(2833-2838)tgtttgfs p.CL945fs CESC 15 59323793 59323793 + Missense_Mutation SNP G G A TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr15:59323793G>A c.772G>A c.(772-774)Gag>Aag p.E258K CESC 15 59344533 59344533 + Missense_Mutation SNP G G C TCGA-UC-A7PF-01A-11D-A351-09 TCGA-UC-A7PF-11A-31D-A351-09 g.chr15:59344533G>C c.910G>C c.(910-912)Gaa>Caa p.E304Q CESC 15 59373346 59373346 + Missense_Mutation SNP C C G TCGA-EK-A2RK-01A-11D-A18J-09 TCGA-EK-A2RK-10A-01D-A18J-09 g.chr15:59373346C>G c.2160C>G c.(2158-2160)atC>atG p.I720M CESC 15 59387098 59387098 + Nonstop_Mutation SNP G G C TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr15:59387098G>C c.2984G>C c.(2983-2985)tGa>tCa p.*995S COAD 15 59323267 59323267 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr15:59323267G>A c.246G>A c.(244-246)caG>caA p.Q82Q COAD 15 59323280 59323280 + Missense_Mutation SNP A A C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr15:59323280A>C c.259A>C c.(259-261)Aaa>Caa p.K87Q COAD 15 59323704 59323705 + Frame_Shift_Del DEL AA AA - TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr15:59323704_59323705delAA c.683_684delAA c.(682-684)caafs p.Q228fs COAD 15 59350567 59350567 + Missense_Mutation SNP T T C TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr15:59350567T>C c.1184T>C c.(1183-1185)gTa>gCa p.V395A COAD 15 59359141 59359141 + Silent SNP T T C TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr15:59359141T>C c.1545T>C c.(1543-1545)caT>caC p.H515H COAD 15 59368182 59368182 + Silent SNP T T C TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr15:59368182T>C c.1716T>C c.(1714-1716)agT>agC p.S572S COAD 15 59368258 59368258 + Nonsense_Mutation SNP C C T TCGA-AA-3852-01A-01W-0900-09 TCGA-AA-3852-10A-01W-0900-09 g.chr15:59368258C>T c.1792C>T c.(1792-1794)Cga>Tga p.R598* COAD 15 59368259 59368259 + Missense_Mutation SNP G G A TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr15:59368259G>A c.1793G>A c.(1792-1794)cGa>cAa p.R598Q COAD 15 59373196 59373196 + Frame_Shift_Del DEL C C - TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr15:59373196delC c.2010delC c.(2008-2010)aacfs p.N670fs COAD 15 59373411 59373412 + Frame_Shift_Del DEL CA CA - TCGA-G4-6626-01A-11D-1771-10 TCGA-G4-6626-10A-01D-1771-10 g.chr15:59373411_59373412delCA c.2225_2226delCA c.(2224-2226)gcafs p.A742fs COAD 15 59376336 59376336 + Missense_Mutation SNP A A G TCGA-AA-3712-01A-21D-1719-10 TCGA-AA-3712-11A-01D-1719-10 g.chr15:59376336A>G c.2306A>G c.(2305-2307)cAt>cGt p.H769R COAD 15 59376343 59376343 + Frame_Shift_Del DEL C C - TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr15:59376343delC c.2313delC c.(2311-2313)cgcfs p.R771fs COAD 15 59376343 59376343 + Frame_Shift_Del DEL C C - TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr15:59376343delC c.2313delC c.(2311-2313)cgcfs p.R771fs COAD 15 59376343 59376343 + Frame_Shift_Del DEL C C - TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr15:59376343delC c.2313delC c.(2311-2313)cgcfs p.R771fs COAD 15 59383297 59383297 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr15:59383297C>T c.2683C>T c.(2683-2685)Cgt>Tgt p.R895C COAD 15 59383324 59383324 + Missense_Mutation SNP A A G TCGA-D5-6532-01A-11D-1719-10 TCGA-D5-6532-10A-01D-1719-10 g.chr15:59383324A>G c.2710A>G c.(2710-2712)Aga>Gga p.R904G COAD 15 59383326 59383326 + Silent SNP A A G TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr15:59383326A>G c.2712A>G c.(2710-2712)agA>agG p.R904R COAD 15 59383326 59383326 + Silent SNP A A G TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr15:59383326A>G c.2712A>G c.(2710-2712)agA>agG p.R904R COAD 15 59383326 59383326 + Silent SNP A A G TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr15:59383326A>G c.2712A>G c.(2710-2712)agA>agG p.R904R COAD 15 59386986 59386986 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:59386986C>A c.2872C>A c.(2872-2874)Ctt>Att p.L958I COAD 15 59386998 59386998 + Missense_Mutation SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr15:59386998C>T c.2884C>T c.(2884-2886)Cac>Tac p.H962Y COADREAD 15 59323267 59323267 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr15:59323267G>A c.246G>A c.(244-246)caG>caA p.Q82Q COADREAD 15 59323280 59323280 + Missense_Mutation SNP A A C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr15:59323280A>C c.259A>C c.(259-261)Aaa>Caa p.K87Q COADREAD 15 59323704 59323705 + Frame_Shift_Del DEL AA AA - TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr15:59323704_59323705delAA c.683_684delAA c.(682-684)caafs p.Q228fs COADREAD 15 59344611 59344611 + Missense_Mutation SNP A A C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:59344611A>C c.988A>C c.(988-990)Aca>Cca p.T330P COADREAD 15 59347929 59347929 + Silent SNP C C A TCGA-DC-6681-01A-11D-1826-10 TCGA-DC-6681-10A-01D-1826-10 g.chr15:59347929C>A c.1056C>A c.(1054-1056)tcC>tcA p.S352S COADREAD 15 59348038 59348038 + Nonsense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr15:59348038G>T c.1165G>T c.(1165-1167)Gaa>Taa p.E389* COADREAD 15 59350567 59350567 + Missense_Mutation SNP T T C TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr15:59350567T>C c.1184T>C c.(1183-1185)gTa>gCa p.V395A COADREAD 15 59359141 59359141 + Silent SNP T T C TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr15:59359141T>C c.1545T>C c.(1543-1545)caT>caC p.H515H COADREAD 15 59359277 59359277 + Nonsense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr15:59359277G>T c.1681G>T c.(1681-1683)Gaa>Taa p.E561* COADREAD 15 59368182 59368182 + Silent SNP T T C TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr15:59368182T>C c.1716T>C c.(1714-1716)agT>agC p.S572S COADREAD 15 59368258 59368258 + Nonsense_Mutation SNP C C T TCGA-AA-3852-01A-01W-0900-09 TCGA-AA-3852-10A-01W-0900-09 g.chr15:59368258C>T c.1792C>T c.(1792-1794)Cga>Tga p.R598* COADREAD 15 59368259 59368259 + Missense_Mutation SNP G G A TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr15:59368259G>A c.1793G>A c.(1792-1794)cGa>cAa p.R598Q COADREAD 15 59373196 59373196 + Frame_Shift_Del DEL C C - TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr15:59373196delC c.2010delC c.(2008-2010)aacfs p.N670fs COADREAD 15 59373358 59373358 + Silent SNP T T C TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chr15:59373358T>C c.2172T>C c.(2170-2172)ctT>ctC p.L724L COADREAD 15 59373411 59373412 + Frame_Shift_Del DEL CA CA - TCGA-G4-6626-01A-11D-1771-10 TCGA-G4-6626-10A-01D-1771-10 g.chr15:59373411_59373412delCA c.2225_2226delCA c.(2224-2226)gcafs p.A742fs COADREAD 15 59376336 59376336 + Missense_Mutation SNP A A G TCGA-AA-3712-01A-21D-1719-10 TCGA-AA-3712-11A-01D-1719-10 g.chr15:59376336A>G c.2306A>G c.(2305-2307)cAt>cGt p.H769R COADREAD 15 59376343 59376343 + Frame_Shift_Del DEL C C - TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr15:59376343delC c.2313delC c.(2311-2313)cgcfs p.R771fs COADREAD 15 59376343 59376343 + Frame_Shift_Del DEL C C - TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr15:59376343delC c.2313delC c.(2311-2313)cgcfs p.R771fs COADREAD 15 59376343 59376343 + Frame_Shift_Del DEL C C - TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr15:59376343delC c.2313delC c.(2311-2313)cgcfs p.R771fs COADREAD 15 59383297 59383297 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr15:59383297C>T c.2683C>T c.(2683-2685)Cgt>Tgt p.R895C COADREAD 15 59383324 59383324 + Missense_Mutation SNP A A G TCGA-D5-6532-01A-11D-1719-10 TCGA-D5-6532-10A-01D-1719-10 g.chr15:59383324A>G c.2710A>G c.(2710-2712)Aga>Gga p.R904G COADREAD 15 59383326 59383326 + Silent SNP A A G TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr15:59383326A>G c.2712A>G c.(2710-2712)agA>agG p.R904R COADREAD 15 59383326 59383326 + Silent SNP A A G TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr15:59383326A>G c.2712A>G c.(2710-2712)agA>agG p.R904R COADREAD 15 59383326 59383326 + Silent SNP A A G TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr15:59383326A>G c.2712A>G c.(2710-2712)agA>agG p.R904R COADREAD 15 59386986 59386986 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:59386986C>A c.2872C>A c.(2872-2874)Ctt>Att p.L958I COADREAD 15 59386998 59386998 + Missense_Mutation SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr15:59386998C>T c.2884C>T c.(2884-2886)Cac>Tac p.H962Y ESCA 15 59323811 59323811 + Nonsense_Mutation SNP G G T TCGA-LN-A9FQ-01A-31D-A387-09 TCGA-LN-A9FQ-10A-01D-A38A-09 g.chr15:59323811G>T c.790G>T c.(790-792)Gaa>Taa p.E264* ESCA 15 59344540 59344540 + Missense_Mutation SNP C C G TCGA-2H-A9GG-01A-11D-A37C-09 TCGA-2H-A9GG-11A-11D-A37F-09 g.chr15:59344540C>G c.917C>G c.(916-918)tCc>tGc p.S306C ESCA 15 59359099 59359099 + Missense_Mutation SNP T T G TCGA-VR-A8EP-01A-31D-A403-09 TCGA-VR-A8EP-10B-01D-A403-09 g.chr15:59359099T>G c.1503T>G c.(1501-1503)caT>caG p.H501Q ESCA 15 59368393 59368393 + Nonsense_Mutation SNP C C T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr15:59368393C>T c.1927C>T c.(1927-1929)Cga>Tga p.R643* ESCA 15 59373162 59373162 + Missense_Mutation SNP A A G TCGA-LN-A9FO-01A-11D-A387-09 TCGA-LN-A9FO-10A-01D-A38A-09 g.chr15:59373162A>G c.1976A>G c.(1975-1977)cAt>cGt p.H659R ESCA 15 59373269 59373269 + Nonsense_Mutation SNP C C T TCGA-LN-A9FP-01A-31D-A387-09 TCGA-LN-A9FP-10A-01D-A38A-09 g.chr15:59373269C>T c.2083C>T c.(2083-2085)Caa>Taa p.Q695* ESCA 15 59383298 59383298 + Missense_Mutation SNP G G A TCGA-V5-AASX-01A-11D-A387-09 TCGA-V5-AASX-10A-01D-A38A-09 g.chr15:59383298G>A c.2684G>A c.(2683-2685)cGt>cAt p.R895H ESCA 15 59383348 59383348 + Frame_Shift_Del DEL A A - TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr15:59383348delA c.2734delA c.(2734-2736)aaafs p.K913fs GBM 15 59323149 59323149 + Missense_Mutation SNP T T C TCGA-32-2634-01A-01D-1495-08 TCGA-32-2634-10A-01D-1495-08 g.chr15:59323149T>C c.128T>C c.(127-129)aTt>aCt p.I43T GBMLGG 15 59323149 59323149 + Missense_Mutation SNP T T C TCGA-32-2634-01A-01D-1495-08 TCGA-32-2634-10A-01D-1495-08 g.chr15:59323149T>C c.128T>C c.(127-129)aTt>aCt p.I43T GBMLGG 15 59373204 59373204 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:59373204C>A c.2018C>A c.(2017-2019)cCt>cAt p.P673H GBMLGG 15 59384789 59384789 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:59384789G>T c.2817G>T c.(2815-2817)gaG>gaT p.E939D HNSC 15 59323315 59323315 + Silent SNP G G A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr15:59323315G>A c.294G>A c.(292-294)caG>caA p.Q98Q HNSC 15 59323323 59323323 + Missense_Mutation SNP G G T TCGA-CN-A63W-01A-11D-A30E-08 TCGA-CN-A63W-10A-01D-A30H-08 g.chr15:59323323G>T c.302G>T c.(301-303)gGc>gTc p.G101V HNSC 15 59350639 59350639 + Missense_Mutation SNP C C G TCGA-4P-AA8J-01A-11D-A391-08 TCGA-4P-AA8J-10A-01D-A394-08 g.chr15:59350639C>G c.1256C>G c.(1255-1257)tCt>tGt p.S419C HNSC 15 59350644 59350644 + Nonsense_Mutation SNP C C T TCGA-CV-7411-01A-11D-2078-08 TCGA-CV-7411-10A-01D-2078-08 g.chr15:59350644C>T c.1261C>T c.(1261-1263)Cag>Tag p.Q421* HNSC 15 59350698 59350698 + Missense_Mutation SNP G G A TCGA-T3-A92N-01A-11D-A391-08 TCGA-T3-A92N-10A-01D-A394-08 g.chr15:59350698G>A c.1315G>A c.(1315-1317)Gag>Aag p.E439K HNSC 15 59359174 59359174 + Silent SNP C C T TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr15:59359174C>T c.1578C>T c.(1576-1578)gtC>gtT p.V526V HNSC 15 59359272 59359272 + Missense_Mutation SNP A A G TCGA-BB-A6UO-01A-12D-A34J-08 TCGA-BB-A6UO-10A-01D-A34M-08 g.chr15:59359272A>G c.1676A>G c.(1675-1677)tAt>tGt p.Y559C HNSC 15 59368279 59368279 + Nonsense_Mutation SNP C C T TCGA-CQ-7064-01A-11D-2394-08 TCGA-CQ-7064-10A-01D-2394-08 g.chr15:59368279C>T c.1813C>T c.(1813-1815)Cag>Tag p.Q605* HNSC 15 59373350 59373350 + Nonsense_Mutation SNP C C T TCGA-CR-6472-01A-11D-1870-08 TCGA-CR-6472-10A-01D-1870-08 g.chr15:59373350C>T c.2164C>T c.(2164-2166)Cag>Tag p.Q722* HNSC 15 59373425 59373425 + Missense_Mutation SNP C C T TCGA-CR-7377-01A-11D-2012-08 TCGA-CR-7377-10A-01D-2013-08 g.chr15:59373425C>T c.2239C>T c.(2239-2241)Cct>Tct p.P747S HNSC 15 59376343 59376343 + Frame_Shift_Del DEL C C - TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr15:59376343delC c.2313delC c.(2311-2313)cgcfs p.R771fs HNSC 15 59383308 59383308 + Silent SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr15:59383308C>T c.2694C>T c.(2692-2694)tcC>tcT p.S898S KICH 15 59368246 59368246 + Missense_Mutation SNP G G T TCGA-KL-8343-01A-11D-2310-10 TCGA-KL-8343-11A-01D-2310-10 g.chr15:59368246G>T c.1780G>T c.(1780-1782)Gtt>Ttt p.V594F KIPAN 15 59344604 59344604 + Missense_Mutation SNP G G T TCGA-A4-A5Y1-01A-11D-A28G-10 TCGA-A4-A5Y1-11A-11D-A28G-10 g.chr15:59344604G>T c.981G>T c.(979-981)gaG>gaT p.E327D KIPAN 15 59350658 59350658 + Silent SNP T T A TCGA-F9-A7VF-01A-11D-A33Q-10 TCGA-F9-A7VF-10A-01D-A33Q-10 g.chr15:59350658T>A c.1275T>A c.(1273-1275)acT>acA p.T425T KIPAN 15 59358971 59358971 + Silent SNP A A C TCGA-SX-A7SP-01A-11D-A34Z-10 TCGA-SX-A7SP-10A-01D-A34Z-10 g.chr15:59358971A>C c.1375A>C c.(1375-1377)Agg>Cgg p.R459R KIPAN 15 59368246 59368246 + Missense_Mutation SNP G G T TCGA-KL-8343-01A-11D-2310-10 TCGA-KL-8343-11A-01D-2310-10 g.chr15:59368246G>T c.1780G>T c.(1780-1782)Gtt>Ttt p.V594F KIRP 15 59344604 59344604 + Missense_Mutation SNP G G T TCGA-A4-A5Y1-01A-11D-A28G-10 TCGA-A4-A5Y1-11A-11D-A28G-10 g.chr15:59344604G>T c.981G>T c.(979-981)gaG>gaT p.E327D KIRP 15 59350658 59350658 + Silent SNP T T A TCGA-F9-A7VF-01A-11D-A33Q-10 TCGA-F9-A7VF-10A-01D-A33Q-10 g.chr15:59350658T>A c.1275T>A c.(1273-1275)acT>acA p.T425T KIRP 15 59358971 59358971 + Silent SNP A A C TCGA-SX-A7SP-01A-11D-A34Z-10 TCGA-SX-A7SP-10A-01D-A34Z-10 g.chr15:59358971A>C c.1375A>C c.(1375-1377)Agg>Cgg p.R459R LAML 15 59368279 59368279 + Nonsense_Mutation SNP C C T TCGA-AB-2905-03A-01D-0739-09 TCGA-AB-2905-11A-01D-0739-09 g.chr15:59368279C>T c.1813C>T c.(1813-1815)Cag>Tag p.Q605* LGG 15 59373204 59373204 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:59373204C>A c.2018C>A c.(2017-2019)cCt>cAt p.P673H LGG 15 59384789 59384789 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:59384789G>T c.2817G>T c.(2815-2817)gaG>gaT p.E939D LIHC 15 59350608 59350608 + Missense_Mutation SNP G G C TCGA-DD-AACI-01A-11D-A40R-10 TCGA-DD-AACI-10A-01D-A40U-10 g.chr15:59350608G>C c.1225G>C c.(1225-1227)Gct>Cct p.A409P LIHC 15 59373264 59373264 + Missense_Mutation SNP A A G TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr15:59373264A>G c.2078A>G c.(2077-2079)cAt>cGt p.H693R LIHC 15 59377873 59377873 + Silent SNP A A G TCGA-G3-A3CG-01A-11D-A20W-10 TCGA-G3-A3CG-10A-01D-A20W-10 g.chr15:59377873A>G c.2439A>G c.(2437-2439)gaA>gaG p.E813E LIHC 15 59381902 59381902 + Missense_Mutation SNP A A G TCGA-DD-AAEG-01A-11D-A38X-10 TCGA-DD-AAEG-10A-01D-A38X-10 g.chr15:59381902A>G c.2587A>G c.(2587-2589)Att>Gtt p.I863V LIHC 15 59383348 59383348 + Frame_Shift_Del DEL A A - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr15:59383348delA c.2734delA c.(2734-2736)aaafs p.K913fs LUAD 15 59323058 59323058 + Missense_Mutation SNP A A G TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chr15:59323058A>G c.37A>G c.(37-39)Acc>Gcc p.T13A LUAD 15 59323235 59323235 + Missense_Mutation SNP C C G TCGA-05-5715-01A-01D-1625-08 TCGA-05-5715-10A-01D-1625-08 g.chr15:59323235C>G c.214C>G c.(214-216)Caa>Gaa p.Q72E LUAD 15 59323899 59323899 + Nonsense_Mutation SNP C C G TCGA-93-8067-01A-11D-2284-08 TCGA-93-8067-10A-01D-2284-08 g.chr15:59323899C>G c.878C>G c.(877-879)tCa>tGa p.S293* LUSC 15 59323142 59323142 + Missense_Mutation SNP G G C TCGA-22-5473-01A-01D-1632-08 TCGA-22-5473-11A-11D-1632-08 g.chr15:59323142G>C c.121G>C c.(121-123)Gag>Cag p.E41Q LUSC 15 59323210 59323210 + Missense_Mutation SNP A A C TCGA-18-3415-01A-01D-0983-08 TCGA-18-3415-11A-01D-0983-08 g.chr15:59323210A>C c.189A>C c.(187-189)gaA>gaC p.E63D LUSC 15 59344503 59344503 + Splice_Site SNP G G A TCGA-22-1016-01A-01D-1521-08 TCGA-22-1016-11A-01D-1521-08 g.chr15:59344503G>A c.e3-1 LUSC 15 59373224 59373224 + Missense_Mutation SNP C C G TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr15:59373224C>G c.2038C>G c.(2038-2040)Caa>Gaa p.Q680E LUSC 15 59373363 59373363 + Missense_Mutation SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr15:59373363C>T c.2177C>T c.(2176-2178)cCt>cTt p.P726L LUSC 15 59377922 59377922 + Silent SNP T T C TCGA-60-2724-01A-01D-1522-08 TCGA-60-2724-11A-01D-1522-08 g.chr15:59377922T>C c.2488T>C c.(2488-2490)Ttg>Ctg p.L830L OV 15 59344631 59344631 + Splice_Site SNP G G T TCGA-36-2548-01A-01D-1526-09 TCGA-36-2548-10A-01D-1526-09 g.chr15:59344631G>T c.e3+1 OV 15 59383326 59383326 + Missense_Mutation SNP A A T TCGA-20-0991-01A-03D-0428-08 TCGA-20-0991-10A-01D-0428-08 g.chr15:59383326A>T c.2712A>T c.(2710-2712)agA>agT p.R904S OV 15 59384740 59384740 + Missense_Mutation SNP A A T TCGA-23-1022-01A-02W-0488-09 TCGA-23-1022-10A-01W-0488-09 g.chr15:59384740A>T c.2768A>T c.(2767-2769)aAa>aTa p.K923I OV 15 59386983 59386983 + Splice_Site SNP C C T TCGA-29-1702-01A-01W-0633-09 TCGA-29-1702-10A-01W-0633-09 g.chr15:59386983C>T c.2869C>T c.(2869-2871)Cgt>Tgt p.R957C PAAD 15 59323801 59323801 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:59323801C>T c.780C>T c.(778-780)gaC>gaT p.D260D PAAD 15 59344625 59344625 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:59344625C>T c.1002C>T c.(1000-1002)agC>agT p.S334S PAAD 15 59359283 59359283 + Splice_Site SNP G G C TCGA-3A-A9I9-01A-11D-A38G-08 TCGA-3A-A9I9-10A-01D-A38J-08 g.chr15:59359283G>C c.e6+1 PAAD 15 59368362 59368362 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:59368362G>T c.1896G>T c.(1894-1896)caG>caT p.Q632H PRAD 15 59377913 59377913 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr15:59377913C>T c.2479C>T c.(2479-2481)Cat>Tat p.H827Y READ 15 59344611 59344611 + Missense_Mutation SNP A A C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:59344611A>C c.988A>C c.(988-990)Aca>Cca p.T330P READ 15 59347929 59347929 + Silent SNP C C A TCGA-DC-6681-01A-11D-1826-10 TCGA-DC-6681-10A-01D-1826-10 g.chr15:59347929C>A c.1056C>A c.(1054-1056)tcC>tcA p.S352S READ 15 59348038 59348038 + Nonsense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr15:59348038G>T c.1165G>T c.(1165-1167)Gaa>Taa p.E389* READ 15 59359277 59359277 + Nonsense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr15:59359277G>T c.1681G>T c.(1681-1683)Gaa>Taa p.E561* READ 15 59373358 59373358 + Silent SNP T T C TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chr15:59373358T>C c.2172T>C c.(2170-2172)ctT>ctC p.L724L SARC 15 59323147 59323147 + Silent SNP C C T TCGA-DX-A8BP-01A-11D-A37C-09 TCGA-DX-A8BP-10A-01D-A37F-09 g.chr15:59323147C>T c.126C>T c.(124-126)ccC>ccT p.P42P SARC 15 59323560 59323560 + Missense_Mutation SNP G G C TCGA-IS-A3K8-01A-11D-A21Q-09 TCGA-IS-A3K8-10A-01D-A21Q-09 g.chr15:59323560G>C c.539G>C c.(538-540)cGg>cCg p.R180P SKCM 15 59323125 59323125 + Missense_Mutation SNP G G A TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr15:59323125G>A c.104G>A c.(103-105)gGg>gAg p.G35E SKCM 15 59323895 59323895 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:59323895C>T c.874C>T c.(874-876)Ccc>Tcc p.P292S SKCM 15 59359153 59359153 + Silent SNP C C T TCGA-EE-A3AH-06A-11D-A196-08 TCGA-EE-A3AH-10A-01D-A198-08 g.chr15:59359153C>T c.1557C>T c.(1555-1557)caC>caT p.H519H SKCM 15 59373179 59373179 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:59373179C>T c.1993C>T c.(1993-1995)Ccg>Tcg p.P665S SKCM 15 59373233 59373233 + Missense_Mutation SNP T T C TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr15:59373233T>C c.2047T>C c.(2047-2049)Tat>Cat p.Y683H SKCM 15 59373248 59373248 + Missense_Mutation SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr15:59373248C>T c.2062C>T c.(2062-2064)Cct>Tct p.P688S SKCM 15 59373296 59373296 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:59373296C>T c.2110C>T c.(2110-2112)Cct>Tct p.P704S SKCM 15 59381920 59381920 + Missense_Mutation SNP G G C TCGA-DA-A1I4-06A-11D-A196-08 TCGA-DA-A1I4-10A-01D-A198-08 g.chr15:59381920G>C c.2605G>C c.(2605-2607)Gga>Cga p.G869R SKCM 15 59383267 59383267 + Missense_Mutation SNP C C T TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr15:59383267C>T c.2653C>T c.(2653-2655)Cat>Tat p.H885Y

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation ALL-US 15 59191792 59191792 single base substitution C T intron_variant BLCA-CN 15 59175958 59175958 single base substitution C T intron_variant BLCA-CN 15 59191787 59191787 single base substitution C T intron_variant BLCA-CN 15 59225668 59225668 single base substitution C T intron_variant BLCA-CN 15 59377858 59377858 single base substitution G C downstream_gene_variant BLCA-CN 15 59377858 59377858 single base substitution G C exon_variant BLCA-CN 15 59377858 59377858 single base substitution G C missense_variant W808C 2424G>C BLCA-CN 15 59377858 59377858 single base substitution G C missense_variant W817C 2451G>C BLCA-CN 15 59377858 59377858 single base substitution G C splice_region_variant BLCA-CN 15 59383301 59383301 single base substitution G A downstream_gene_variant BLCA-CN 15 59383301 59383301 single base substitution G A exon_variant BLCA-CN 15 59383301 59383301 single base substitution G A missense_variant G896E 2687G>A BLCA-CN 15 59383301 59383301 single base substitution G A missense_variant G905E 2714G>A BLCA-CN 15 59383301 59383301 single base substitution G A upstream_gene_variant BLCA-US 15 59179635 59179635 single base substitution C T intron_variant BLCA-US 15 59179725 59179725 single base substitution A T intron_variant BLCA-US 15 59182564 59182565 deletion of <=200bp CT - intron_variant BLCA-US 15 59191829 59191829 single base substitution C A intron_variant BLCA-US 15 59323779 59323779 single base substitution C G downstream_gene_variant BLCA-US 15 59323779 59323779 single base substitution C G missense_variant S253C 758C>G BLCA-US 15 59323779 59323779 single base substitution C G upstream_gene_variant BLCA-US 15 59344515 59344515 single base substitution G A missense_variant E298K 892G>A BLCA-US 15 59344515 59344515 single base substitution G A missense_variant E31K 91G>A BLCA-US 15 59350651 59350651 single base substitution C T missense_variant S156F 467C>T BLCA-US 15 59350651 59350651 single base substitution C T missense_variant S423F 1268C>T BLCA-US 15 59350705 59350705 single base substitution C T missense_variant S174L 521C>T BLCA-US 15 59350705 59350705 single base substitution C T missense_variant S441L 1322C>T BLCA-US 15 59350741 59350741 single base substitution C G missense_variant S186C 557C>G BLCA-US 15 59350741 59350741 single base substitution C G missense_variant S453C 1358C>G BLCA-US 15 59358969 59358969 single base substitution C G stop_gained S458* 1373C>G BOCA-FR 15 59310278 59310278 single base substitution A T intron_variant BOCA-FR 15 59377486 59377486 single base substitution C G downstream_gene_variant BOCA-FR 15 59377486 59377486 single base substitution C G intron_variant BOCA-FR 15 59377486 59377486 single base substitution C G upstream_gene_variant BRCA-EU 15 59152427 59152427 single base substitution G C upstream_gene_variant BRCA-EU 15 59153393 59153393 single base substitution G T upstream_gene_variant BRCA-EU 15 59153418 59153418 single base substitution G A upstream_gene_variant BRCA-EU 15 59154492 59154492 single base substitution G T upstream_gene_variant BRCA-EU 15 59154710 59154710 single base substitution G C upstream_gene_variant BRCA-EU 15 59154900 59154900 single base substitution G A upstream_gene_variant BRCA-EU 15 59155346 59155346 single base substitution G A upstream_gene_variant BRCA-EU 15 59157884 59157884 single base substitution C A intron_variant BRCA-EU 15 59158355 59158355 single base substitution T C intron_variant BRCA-EU 15 59159474 59159474 single base substitution T G intron_variant BRCA-EU 15 59159865 59159865 single base substitution T A intron_variant BRCA-EU 15 59161833 59161833 single base substitution C T intron_variant BRCA-EU 15 59161955 59161955 single base substitution T A intron_variant BRCA-EU 15 59163655 59163655 single base substitution A G intron_variant BRCA-EU 15 59163675 59163675 single base substitution C G intron_variant BRCA-EU 15 59164049 59164049 single base substitution A C intron_variant BRCA-EU 15 59164481 59164481 single base substitution G A intron_variant BRCA-EU 15 59165278 59165278 single base substitution C T intron_variant BRCA-EU 15 59165656 59165656 single base substitution G C intron_variant BRCA-EU 15 59165900 59165900 single base substitution C T intron_variant BRCA-EU 15 59166869 59166889 deletion of <=200bp CAAGGGCCTTCCCTGTAGTAC - intron_variant BRCA-EU 15 59171209 59171209 single base substitution C T intron_variant BRCA-EU 15 59172494 59172494 single base substitution C A intron_variant BRCA-EU 15 59173550 59173550 single base substitution C A intron_variant BRCA-EU 15 59174024 59174024 single base substitution C A intron_variant BRCA-EU 15 59175592 59175592 single base substitution C T intron_variant BRCA-EU 15 59176192 59176192 single base substitution G C intron_variant BRCA-EU 15 59176358 59176358 single base substitution T C intron_variant BRCA-EU 15 59177030 59177030 single base substitution C T intron_variant BRCA-EU 15 59178627 59178627 single base substitution G A intron_variant BRCA-EU 15 59178747 59178747 deletion of <=200bp A - intron_variant BRCA-EU 15 59178751 59178751 single base substitution T G intron_variant BRCA-EU 15 59178987 59178987 single base substitution C G intron_variant BRCA-EU 15 59179899 59179899 single base substitution C G intron_variant BRCA-EU 15 59180085 59180085 single base substitution C G intron_variant BRCA-EU 15 59180352 59180352 deletion of <=200bp A - intron_variant BRCA-EU 15 59181165 59181165 single base substitution C A intron_variant BRCA-EU 15 59183542 59183542 single base substitution C T intron_variant BRCA-EU 15 59186547 59186547 single base substitution C T intron_variant BRCA-EU 15 59186570 59186570 single base substitution C T intron_variant BRCA-EU 15 59188569 59188569 single base substitution C T intron_variant BRCA-EU 15 59190265 59190265 single base substitution A T intron_variant BRCA-EU 15 59192217 59192217 single base substitution G C intron_variant BRCA-EU 15 59195245 59195245 single base substitution C T intron_variant BRCA-EU 15 59196381 59196381 insertion of <=200bp - T intron_variant BRCA-EU 15 59196731 59196731 single base substitution T C intron_variant BRCA-EU 15 59197876 59197876 deletion of <=200bp A - intron_variant BRCA-EU 15 59200881 59200881 single base substitution C G intron_variant BRCA-EU 15 59201929 59201929 single base substitution G C intron_variant BRCA-EU 15 59202333 59202333 single base substitution G A intron_variant BRCA-EU 15 59202838 59202838 single base substitution A G intron_variant BRCA-EU 15 59203517 59203517 single base substitution A T intron_variant BRCA-EU 15 59205271 59205271 single base substitution G A intron_variant BRCA-EU 15 59205678 59205678 deletion of <=200bp A - intron_variant BRCA-EU 15 59205822 59205822 single base substitution C G intron_variant BRCA-EU 15 59206135 59206135 single base substitution T C intron_variant BRCA-EU 15 59207741 59207741 single base substitution G C intron_variant BRCA-EU 15 59208110 59208110 single base substitution C T intron_variant BRCA-EU 15 59208761 59208761 single base substitution A G intron_variant BRCA-EU 15 59209717 59209717 single base substitution C G intron_variant BRCA-EU 15 59209719 59209719 single base substitution C T intron_variant BRCA-EU 15 59210644 59210644 single base substitution C G intron_variant BRCA-EU 15 59211256 59211256 single base substitution G A intron_variant BRCA-EU 15 59211639 59211639 single base substitution A T intron_variant BRCA-EU 15 59213078 59213078 single base substitution C T intron_variant BRCA-EU 15 59213511 59213511 single base substitution C T intron_variant BRCA-EU 15 59218875 59218875 single base substitution A G intron_variant BRCA-EU 15 59219431 59219431 insertion of <=200bp - T intron_variant BRCA-EU 15 59220986 59220986 single base substitution G A intron_variant BRCA-EU 15 59221854 59221854 single base substitution G A intron_variant BRCA-EU 15 59222595 59222595 single base substitution C A intron_variant BRCA-EU 15 59223603 59223603 single base substitution A G intron_variant BRCA-EU 15 59224033 59224033 single base substitution C G intron_variant BRCA-EU 15 59224171 59224171 single base substitution G C intron_variant BRCA-EU 15 59225814 59225814 single base substitution G A intron_variant BRCA-EU 15 59226454 59226454 single base substitution C G intron_variant BRCA-EU 15 59226857 59226857 deletion of <=200bp A - intron_variant BRCA-EU 15 59228529 59228529 single base substitution C T intron_variant BRCA-EU 15 59230531 59230531 single base substitution C G intron_variant BRCA-EU 15 59230554 59230554 single base substitution C A intron_variant BRCA-EU 15 59232197 59232197 single base substitution G A intron_variant BRCA-EU 15 59233848 59233848 single base substitution C T intron_variant BRCA-EU 15 59233974 59233974 deletion of <=200bp A - intron_variant BRCA-EU 15 59233980 59233980 single base substitution G C intron_variant BRCA-EU 15 59235230 59235230 single base substitution A T intron_variant BRCA-EU 15 59235489 59235489 single base substitution A G intron_variant BRCA-EU 15 59235920 59235920 deletion of <=200bp A - intron_variant BRCA-EU 15 59235920 59235920 insertion of <=200bp - A intron_variant BRCA-EU 15 59237447 59237447 single base substitution C A intron_variant BRCA-EU 15 59238458 59238458 single base substitution C T intron_variant BRCA-EU 15 59239614 59239614 single base substitution T A intron_variant BRCA-EU 15 59239638 59239638 single base substitution G A intron_variant BRCA-EU 15 59239785 59239785 single base substitution A T intron_variant BRCA-EU 15 59241034 59241034 single base substitution G A intron_variant BRCA-EU 15 59241296 59241296 single base substitution G A intron_variant BRCA-EU 15 59246802 59246802 single base substitution T A intron_variant BRCA-EU 15 59247279 59247279 single base substitution A T intron_variant BRCA-EU 15 59247869 59247869 single base substitution T G intron_variant BRCA-EU 15 59248373 59248373 single base substitution G A intron_variant BRCA-EU 15 59248614 59248614 single base substitution C G intron_variant BRCA-EU 15 59248707 59248707 single base substitution C G intron_variant BRCA-EU 15 59249525 59249525 single base substitution C A intron_variant BRCA-EU 15 59250087 59250087 single base substitution G T intron_variant BRCA-EU 15 59252297 59252297 deletion of <=200bp G - intron_variant BRCA-EU 15 59253870 59253870 single base substitution G T intron_variant BRCA-EU 15 59258262 59258262 single base substitution C T intron_variant BRCA-EU 15 59260615 59260615 single base substitution C G intron_variant BRCA-EU 15 59260806 59260806 single base substitution C G intron_variant BRCA-EU 15 59262212 59262212 single base substitution G T intron_variant BRCA-EU 15 59263968 59263968 single base substitution G A intron_variant BRCA-EU 15 59264217 59264217 single base substitution G A intron_variant BRCA-EU 15 59264549 59264549 single base substitution A G intron_variant BRCA-EU 15 59264879 59264879 single base substitution C T intron_variant BRCA-EU 15 59266360 59266360 single base substitution C T intron_variant BRCA-EU 15 59266513 59266543 deletion of <=200bp ATTTTTCTTTCAGACAGAGTCTCATTCTGTC - intron_variant BRCA-EU 15 59267202 59267202 single base substitution C G intron_variant BRCA-EU 15 59267345 59267345 single base substitution A G intron_variant BRCA-EU 15 59267796 59267796 single base substitution C G intron_variant BRCA-EU 15 59267954 59267954 single base substitution C G intron_variant BRCA-EU 15 59269666 59269666 single base substitution C G intron_variant BRCA-EU 15 59270691 59270691 single base substitution C G intron_variant BRCA-EU 15 59273678 59273678 insertion of <=200bp - T intron_variant BRCA-EU 15 59274715 59274715 single base substitution C G intron_variant BRCA-EU 15 59275139 59275139 single base substitution G A intron_variant BRCA-EU 15 59275139 59275139 single base substitution G A upstream_gene_variant BRCA-EU 15 59275848 59275848 single base substitution C T intron_variant BRCA-EU 15 59275848 59275848 single base substitution C T upstream_gene_variant BRCA-EU 15 59275953 59275953 single base substitution C A intron_variant BRCA-EU 15 59275953 59275953 single base substitution C A upstream_gene_variant BRCA-EU 15 59276387 59276387 single base substitution G C intron_variant BRCA-EU 15 59276387 59276387 single base substitution G C upstream_gene_variant BRCA-EU 15 59278861 59278861 single base substitution C G intron_variant BRCA-EU 15 59278861 59278861 single base substitution C G upstream_gene_variant BRCA-EU 15 59278862 59278862 single base substitution C T intron_variant BRCA-EU 15 59278862 59278862 single base substitution C T upstream_gene_variant BRCA-EU 15 59279751 59279751 insertion of <=200bp - G intron_variant BRCA-EU 15 59279751 59279751 insertion of <=200bp - G upstream_gene_variant BRCA-EU 15 59280019 59280019 single base substitution C T 5_prime_UTR_variant BRCA-EU 15 59280019 59280019 single base substitution C T intron_variant BRCA-EU 15 59280019 59280019 single base substitution C T upstream_gene_variant BRCA-EU 15 59281654 59281654 single base substitution C G intron_variant BRCA-EU 15 59281741 59281741 single base substitution C G intron_variant BRCA-EU 15 59282280 59282280 single base substitution T G intron_variant BRCA-EU 15 59284524 59284524 single base substitution G A intron_variant BRCA-EU 15 59284728 59284728 insertion of <=200bp - T intron_variant BRCA-EU 15 59285226 59285226 single base substitution G A intron_variant BRCA-EU 15 59286267 59286267 single base substitution C T intron_variant BRCA-EU 15 59286307 59286307 single base substitution G A intron_variant BRCA-EU 15 59289357 59289357 deletion of <=200bp A - intron_variant BRCA-EU 15 59290011 59290011 single base substitution C G intron_variant BRCA-EU 15 59290252 59290252 single base substitution T C intron_variant BRCA-EU 15 59291071 59291071 single base substitution G A intron_variant BRCA-EU 15 59292133 59292133 single base substitution C G intron_variant BRCA-EU 15 59292558 59292558 single base substitution C T intron_variant BRCA-EU 15 59292609 59292609 single base substitution A G intron_variant BRCA-EU 15 59294832 59294832 single base substitution T G intron_variant BRCA-EU 15 59295138 59295139 deletion of <=200bp AG - intron_variant BRCA-EU 15 59296316 59296316 single base substitution C T 5_prime_UTR_variant BRCA-EU 15 59296316 59296316 single base substitution C T intron_variant BRCA-EU 15 59297622 59297622 single base substitution A T intron_variant BRCA-EU 15 59298400 59298400 single base substitution T G intron_variant BRCA-EU 15 59299077 59299077 single base substitution C T intron_variant BRCA-EU 15 59299546 59299546 single base substitution C T intron_variant BRCA-EU 15 59299767 59299767 single base substitution G A intron_variant BRCA-EU 15 59299768 59299768 single base substitution G T intron_variant BRCA-EU 15 59300055 59300055 single base substitution A G intron_variant BRCA-EU 15 59301562 59301562 single base substitution C A intron_variant BRCA-EU 15 59305157 59305157 single base substitution T C intron_variant BRCA-EU 15 59305229 59305229 deletion of <=200bp C - intron_variant BRCA-EU 15 59308406 59308406 single base substitution G A intron_variant BRCA-EU 15 59309711 59309711 single base substitution A G intron_variant BRCA-EU 15 59310603 59310603 single base substitution C T intron_variant BRCA-EU 15 59310708 59310708 insertion of <=200bp - A intron_variant BRCA-EU 15 59312229 59312229 single base substitution A T intron_variant BRCA-EU 15 59317043 59317043 single base substitution C T intron_variant BRCA-EU 15 59317879 59317879 single base substitution A T intron_variant BRCA-EU 15 59318121 59318121 deletion of <=200bp T - intron_variant BRCA-EU 15 59318121 59318121 deletion of <=200bp T - upstream_gene_variant BRCA-EU 15 59319112 59319112 deletion of <=200bp C - intron_variant BRCA-EU 15 59319112 59319112 deletion of <=200bp C - upstream_gene_variant BRCA-EU 15 59321994 59321994 single base substitution C G intron_variant BRCA-EU 15 59321994 59321994 single base substitution C G upstream_gene_variant BRCA-EU 15 59322129 59322129 single base substitution T C intron_variant BRCA-EU 15 59322129 59322129 single base substitution T C upstream_gene_variant BRCA-EU 15 59322539 59322539 single base substitution G A intron_variant BRCA-EU 15 59322539 59322539 single base substitution G A upstream_gene_variant BRCA-EU 15 59322933 59322933 single base substitution A G intron_variant BRCA-EU 15 59322933 59322933 single base substitution A G upstream_gene_variant BRCA-EU 15 59324618 59324618 insertion of <=200bp - T downstream_gene_variant BRCA-EU 15 59324618 59324618 insertion of <=200bp - T intron_variant BRCA-EU 15 59324632 59324632 insertion of <=200bp - T downstream_gene_variant BRCA-EU 15 59324632 59324632 insertion of <=200bp - T intron_variant BRCA-EU 15 59324837 59324837 single base substitution C G downstream_gene_variant BRCA-EU 15 59324837 59324837 single base substitution C G intron_variant BRCA-EU 15 59325089 59325090 deletion of <=200bp CT - downstream_gene_variant BRCA-EU 15 59325089 59325090 deletion of <=200bp CT - intron_variant BRCA-EU 15 59326232 59326232 single base substitution C T downstream_gene_variant BRCA-EU 15 59326232 59326232 single base substitution C T intron_variant BRCA-EU 15 59327077 59327077 single base substitution G T downstream_gene_variant BRCA-EU 15 59327077 59327077 single base substitution G T intron_variant BRCA-EU 15 59330086 59330086 single base substitution A T intron_variant BRCA-EU 15 59330461 59330461 single base substitution C G intron_variant BRCA-EU 15 59330635 59330635 single base substitution C A intron_variant BRCA-EU 15 59330825 59330825 single base substitution C G intron_variant BRCA-EU 15 59330875 59330875 single base substitution C T intron_variant BRCA-EU 15 59339189 59339189 single base substitution C G intron_variant BRCA-EU 15 59339861 59339861 single base substitution G A intron_variant BRCA-EU 15 59343499 59343499 deletion of <=200bp A - intron_variant BRCA-EU 15 59346101 59346101 single base substitution G A intron_variant BRCA-EU 15 59347092 59347092 single base substitution C T intron_variant BRCA-EU 15 59347664 59347664 single base substitution C T intron_variant BRCA-EU 15 59347728 59347728 single base substitution A G intron_variant BRCA-EU 15 59348957 59348957 single base substitution T C intron_variant BRCA-EU 15 59353553 59353553 single base substitution C G downstream_gene_variant BRCA-EU 15 59353553 59353553 single base substitution C G intron_variant BRCA-EU 15 59354114 59354114 single base substitution C T downstream_gene_variant BRCA-EU 15 59354114 59354114 single base substitution C T intron_variant BRCA-EU 15 59354910 59354910 single base substitution T C downstream_gene_variant BRCA-EU 15 59354910 59354910 single base substitution T C intron_variant BRCA-EU 15 59356387 59356387 single base substitution G A intron_variant BRCA-EU 15 59356652 59356652 single base substitution G A intron_variant BRCA-EU 15 59358735 59358735 single base substitution G C intron_variant BRCA-EU 15 59358946 59358946 deletion of <=200bp T - intron_variant BRCA-EU 15 59359528 59359528 single base substitution C T intron_variant BRCA-EU 15 59359885 59359885 deletion of <=200bp T - intron_variant BRCA-EU 15 59360895 59360895 single base substitution T C intron_variant BRCA-EU 15 59363547 59363547 single base substitution A G intron_variant BRCA-EU 15 59366587 59366587 single base substitution G T intron_variant BRCA-EU 15 59367801 59367801 single base substitution G C intron_variant BRCA-EU 15 59369790 59369790 single base substitution C T intron_variant BRCA-EU 15 59369790 59369790 single base substitution C T upstream_gene_variant BRCA-EU 15 59372925 59372925 single base substitution A G intron_variant BRCA-EU 15 59372925 59372925 single base substitution A G upstream_gene_variant BRCA-EU 15 59373001 59373001 single base substitution G C intron_variant BRCA-EU 15 59373001 59373001 single base substitution G C upstream_gene_variant BRCA-EU 15 59374612 59374612 single base substitution C T intron_variant BRCA-EU 15 59374612 59374612 single base substitution C T upstream_gene_variant BRCA-EU 15 59374938 59374938 single base substitution A G intron_variant BRCA-EU 15 59374938 59374938 single base substitution A G upstream_gene_variant BRCA-EU 15 59375173 59375173 single base substitution A G intron_variant BRCA-EU 15 59375173 59375173 single base substitution A G upstream_gene_variant BRCA-EU 15 59376343 59376343 deletion of <=200bp C - exon_variant BRCA-EU 15 59376343 59376343 deletion of <=200bp C - frameshift_variant R771 BRCA-EU 15 59376343 59376343 deletion of <=200bp C - frameshift_variant R780 BRCA-EU 15 59376343 59376343 deletion of <=200bp C - upstream_gene_variant BRCA-EU 15 59377146 59377146 single base substitution C T downstream_gene_variant BRCA-EU 15 59377146 59377146 single base substitution C T intron_variant BRCA-EU 15 59377146 59377146 single base substitution C T upstream_gene_variant BRCA-EU 15 59377407 59377407 single base substitution C T downstream_gene_variant BRCA-EU 15 59377407 59377407 single base substitution C T intron_variant BRCA-EU 15 59377407 59377407 single base substitution C T upstream_gene_variant BRCA-EU 15 59378846 59378846 single base substitution C G downstream_gene_variant BRCA-EU 15 59378846 59378846 single base substitution C G intron_variant BRCA-EU 15 59379044 59379044 single base substitution C T downstream_gene_variant BRCA-EU 15 59379044 59379044 single base substitution C T intron_variant BRCA-EU 15 59379455 59379455 single base substitution G C downstream_gene_variant BRCA-EU 15 59379455 59379455 single base substitution G C intron_variant BRCA-EU 15 59380236 59380236 single base substitution G A downstream_gene_variant BRCA-EU 15 59380236 59380236 single base substitution G A intron_variant BRCA-EU 15 59381368 59381368 single base substitution C T downstream_gene_variant BRCA-EU 15 59381368 59381368 single base substitution C T intron_variant BRCA-EU 15 59381368 59381368 single base substitution C T upstream_gene_variant BRCA-EU 15 59383914 59383914 single base substitution C T downstream_gene_variant BRCA-EU 15 59383914 59383914 single base substitution C T intron_variant BRCA-EU 15 59383914 59383914 single base substitution C T upstream_gene_variant BRCA-EU 15 59384526 59384526 single base substitution G C downstream_gene_variant BRCA-EU 15 59384526 59384526 single base substitution G C intron_variant BRCA-EU 15 59384526 59384526 single base substitution G C upstream_gene_variant BRCA-EU 15 59385929 59385929 single base substitution C T downstream_gene_variant BRCA-EU 15 59385929 59385929 single base substitution C T intron_variant BRCA-EU 15 59386921 59386921 single base substitution G T downstream_gene_variant BRCA-EU 15 59386921 59386921 single base substitution G T intron_variant BRCA-EU 15 59387312 59387312 deletion of <=200bp T - 3_prime_UTR_variant BRCA-EU 15 59387312 59387312 deletion of <=200bp T - downstream_gene_variant BRCA-EU 15 59387312 59387312 deletion of <=200bp T - exon_variant BRCA-EU 15 59391505 59391505 single base substitution T C downstream_gene_variant BRCA-EU 15 59392439 59392439 single base substitution C A downstream_gene_variant BRCA-EU 15 59393428 59393429 deletion of <=200bp AG - downstream_gene_variant BRCA-EU 15 59394250 59394250 single base substitution G A downstream_gene_variant BRCA-FR 15 59186547 59186547 single base substitution C T intron_variant BRCA-FR 15 59192217 59192217 single base substitution G C intron_variant BRCA-FR 15 59200881 59200881 single base substitution C G intron_variant BRCA-FR 15 59202838 59202838 single base substitution A G intron_variant BRCA-FR 15 59206135 59206135 single base substitution T C intron_variant BRCA-FR 15 59208110 59208110 single base substitution C T intron_variant BRCA-FR 15 59213511 59213511 single base substitution C T intron_variant BRCA-FR 15 59219371 59219371 single base substitution G A intron_variant BRCA-FR 15 59237079 59237079 single base substitution G C intron_variant BRCA-FR 15 59260615 59260615 single base substitution C G intron_variant BRCA-FR 15 59260806 59260806 single base substitution C G intron_variant BRCA-FR 15 59264549 59264549 single base substitution A G intron_variant BRCA-FR 15 59267954 59267954 single base substitution C G intron_variant BRCA-FR 15 59269666 59269666 single base substitution C G intron_variant BRCA-FR 15 59275848 59275848 single base substitution C T intron_variant BRCA-FR 15 59275848 59275848 single base substitution C T upstream_gene_variant BRCA-FR 15 59275953 59275953 single base substitution C A intron_variant BRCA-FR 15 59275953 59275953 single base substitution C A upstream_gene_variant BRCA-FR 15 59310603 59310603 single base substitution C T intron_variant BRCA-FR 15 59317043 59317043 single base substitution C T intron_variant BRCA-FR 15 59321994 59321994 single base substitution C G intron_variant BRCA-FR 15 59321994 59321994 single base substitution C G upstream_gene_variant BRCA-FR 15 59330825 59330825 single base substitution C G intron_variant BRCA-FR 15 59347092 59347092 single base substitution C T intron_variant BRCA-FR 15 59353553 59353553 single base substitution C G downstream_gene_variant BRCA-FR 15 59353553 59353553 single base substitution C G intron_variant BRCA-FR 15 59356387 59356387 single base substitution G A intron_variant BRCA-FR 15 59374612 59374612 single base substitution C T intron_variant BRCA-FR 15 59374612 59374612 single base substitution C T upstream_gene_variant BRCA-FR 15 59387868 59387868 single base substitution G A 3_prime_UTR_variant BRCA-FR 15 59387868 59387868 single base substitution G A downstream_gene_variant BRCA-FR 15 59387868 59387868 single base substitution G A exon_variant BRCA-FR 15 59389016 59389016 single base substitution G A 3_prime_UTR_variant BRCA-FR 15 59389016 59389016 single base substitution G A downstream_gene_variant BRCA-UK 15 59159474 59159474 single base substitution T G intron_variant BRCA-UK 15 59164049 59164049 single base substitution A C intron_variant BRCA-UK 15 59165278 59165278 single base substitution C T intron_variant BRCA-UK 15 59177030 59177030 single base substitution C T intron_variant BRCA-UK 15 59180263 59180263 single base substitution G C intron_variant BRCA-UK 15 59182088 59182088 single base substitution G A intron_variant BRCA-UK 15 59182647 59182647 single base substitution C T intron_variant BRCA-UK 15 59202333 59202333 single base substitution G A intron_variant BRCA-UK 15 59220986 59220986 single base substitution G A intron_variant BRCA-UK 15 59221815 59221815 single base substitution G C intron_variant BRCA-UK 15 59233980 59233980 single base substitution G C intron_variant BRCA-UK 15 59239614 59239614 single base substitution T A intron_variant BRCA-UK 15 59241296 59241296 single base substitution G A intron_variant BRCA-UK 15 59263968 59263968 single base substitution G A intron_variant BRCA-UK 15 59275139 59275139 single base substitution G A intron_variant BRCA-UK 15 59275139 59275139 single base substitution G A upstream_gene_variant BRCA-UK 15 59291071 59291071 single base substitution G A intron_variant BRCA-UK 15 59299077 59299077 single base substitution C T intron_variant BRCA-UK 15 59319722 59319722 single base substitution A T intron_variant BRCA-UK 15 59319722 59319722 single base substitution A T upstream_gene_variant BRCA-UK 15 59334160 59334160 single base substitution A T intron_variant BRCA-UK 15 59358735 59358735 single base substitution G C intron_variant BRCA-UK 15 59372925 59372925 single base substitution A G intron_variant BRCA-UK 15 59372925 59372925 single base substitution A G upstream_gene_variant BRCA-UK 15 59379044 59379044 single base substitution C T downstream_gene_variant BRCA-UK 15 59379044 59379044 single base substitution C T intron_variant BRCA-UK 15 59394250 59394250 single base substitution G A downstream_gene_variant BRCA-US 15 59175919 59175919 single base substitution A C intron_variant BRCA-US 15 59179738 59179738 single base substitution G A intron_variant BRCA-US 15 59182525 59182526 deletion of <=200bp TC - intron_variant BRCA-US 15 59186732 59186732 single base substitution C T intron_variant BRCA-US 15 59191708 59191708 single base substitution T C intron_variant BRCA-US 15 59205704 59205704 single base substitution T A intron_variant BRCA-US 15 59209183 59209183 single base substitution G T intron_variant BRCA-US 15 59323149 59323149 single base substitution T A missense_variant I43N 128T>A BRCA-US 15 59323149 59323149 single base substitution T A missense_variant I66N 197T>A BRCA-US 15 59323149 59323149 single base substitution T A upstream_gene_variant BRCA-US 15 59323732 59323732 single base substitution G T downstream_gene_variant BRCA-US 15 59323732 59323732 single base substitution G T missense_variant K237N 711G>T BRCA-US 15 59323732 59323732 single base substitution G T upstream_gene_variant BRCA-US 15 59347900 59347900 single base substitution C T missense_variant H343Y 1027C>T BRCA-US 15 59347900 59347900 single base substitution C T missense_variant H76Y 226C>T BRCA-US 15 59350671 59350671 single base substitution A C missense_variant T163P 487A>C BRCA-US 15 59350671 59350671 single base substitution A C missense_variant T430P 1288A>C BRCA-US 15 59359165 59359165 deletion of <=200bp C - frameshift_variant H523 BRCA-US 15 59368259 59368259 single base substitution G A missense_variant R598Q 1793G>A BRCA-US 15 59368259 59368259 single base substitution G A upstream_gene_variant BRCA-US 15 59368377 59368380 deletion of <=200bp CTCT - frameshift_variant PS637 BRCA-US 15 59368377 59368380 deletion of <=200bp CTCT - upstream_gene_variant BRCA-US 15 59373484 59373484 single base substitution G A splice_donor_variant BRCA-US 15 59373484 59373484 single base substitution G A upstream_gene_variant BRCA-US 15 59377902 59377902 single base substitution C T downstream_gene_variant BRCA-US 15 59377902 59377902 single base substitution C T exon_variant BRCA-US 15 59377902 59377902 single base substitution C T missense_variant P823L 2468C>T BRCA-US 15 59377902 59377902 single base substitution C T missense_variant P832L 2495C>T BRCA-US 15 59384805 59384808 deletion of <=200bp TGTT - downstream_gene_variant BRCA-US 15 59384805 59384808 deletion of <=200bp TGTT - exon_variant BRCA-US 15 59384805 59384808 deletion of <=200bp TGTT - frameshift_variant CL937 BRCA-US 15 59384805 59384808 deletion of <=200bp TGTT - frameshift_variant CL945 BRCA-US 15 59384805 59384808 deletion of <=200bp TGTT - frameshift_variant CL946 BRCA-US 15 59384805 59384808 deletion of <=200bp TGTT - frameshift_variant CL954 BRCA-US 15 59384805 59384808 deletion of <=200bp TGTT - upstream_gene_variant BTCA-JP 15 59172304 59172304 single base substitution T C intron_variant BTCA-JP 15 59179551 59179551 single base substitution G A intron_variant BTCA-JP 15 59182490 59182490 single base substitution C A intron_variant BTCA-JP 15 59323399 59323399 single base substitution T C downstream_gene_variant BTCA-JP 15 59323399 59323399 single base substitution T C synonymous_variant S126S 378T>C BTCA-JP 15 59323399 59323399 single base substitution T C upstream_gene_variant BTCA-JP 15 59323623 59323623 single base substitution G T downstream_gene_variant BTCA-JP 15 59323623 59323623 single base substitution G T missense_variant C201F 602G>T BTCA-JP 15 59323623 59323623 single base substitution G T upstream_gene_variant BTCA-JP 15 59347961 59347961 single base substitution G A missense_variant R363Q 1088G>A BTCA-JP 15 59347961 59347961 single base substitution G A missense_variant R96Q 287G>A BTCA-JP 15 59373488 59373488 single base substitution G T intron_variant BTCA-JP 15 59373488 59373488 single base substitution G T splice_region_variant BTCA-JP 15 59373488 59373488 single base substitution G T upstream_gene_variant CESC-US 15 59182658 59182658 single base substitution C T intron_variant CESC-US 15 59186369 59186369 single base substitution T C intron_variant CESC-US 15 59191016 59191016 single base substitution G C intron_variant CESC-US 15 59323793 59323793 single base substitution G A downstream_gene_variant CESC-US 15 59323793 59323793 single base substitution G A missense_variant E258K 772G>A CESC-US 15 59323793 59323793 single base substitution G A upstream_gene_variant CESC-US 15 59344533 59344533 single base substitution G C missense_variant E304Q 910G>C CESC-US 15 59344533 59344533 single base substitution G C missense_variant E37Q 109G>C CESC-US 15 59373346 59373346 single base substitution C G exon_variant CESC-US 15 59373346 59373346 single base substitution C G missense_variant I720M 2160C>G CESC-US 15 59373346 59373346 single base substitution C G upstream_gene_variant CESC-US 15 59387098 59387098 single base substitution G C downstream_gene_variant CESC-US 15 59387098 59387098 single base substitution G C exon_variant CESC-US 15 59387098 59387098 single base substitution G C stop_lost *1004S 3011G>C CESC-US 15 59387098 59387098 single base substitution G C stop_lost *987S 2960G>C CESC-US 15 59387098 59387098 single base substitution G C stop_lost *995S 2984G>C CESC-US 15 59387098 59387098 single base substitution G C stop_lost *996S 2987G>C CESC-US 15 59387291 59387291 insertion of <=200bp - T 3_prime_UTR_variant CESC-US 15 59387291 59387291 insertion of <=200bp - T downstream_gene_variant CESC-US 15 59387291 59387291 insertion of <=200bp - T exon_variant CESC-US 15 59387334 59387334 insertion of <=200bp - T 3_prime_UTR_variant CESC-US 15 59387334 59387334 insertion of <=200bp - T downstream_gene_variant CESC-US 15 59387334 59387334 insertion of <=200bp - T exon_variant CLLE-ES 15 59180312 59180312 single base substitution A G intron_variant CLLE-ES 15 59196104 59196104 single base substitution T A intron_variant CLLE-ES 15 59200464 59200464 single base substitution T A intron_variant CLLE-ES 15 59208899 59208899 single base substitution G A intron_variant CLLE-ES 15 59213548 59213549 multiple base substitution (>=2bp and <=200bp) GA TT intron_variant CLLE-ES 15 59225614 59225614 single base substitution G T intron_variant CLLE-ES 15 59242167 59242167 single base substitution G A intron_variant CLLE-ES 15 59281476 59281481 deletion of <=200bp CTTTTA - intron_variant CLLE-ES 15 59281693 59281693 single base substitution C A intron_variant CLLE-ES 15 59307663 59307663 single base substitution C G intron_variant CLLE-ES 15 59307941 59307941 single base substitution T C intron_variant CLLE-ES 15 59317691 59317691 single base substitution G T intron_variant CLLE-ES 15 59327476 59327476 single base substitution C T downstream_gene_variant CLLE-ES 15 59327476 59327476 single base substitution C T intron_variant CLLE-ES 15 59363999 59363999 single base substitution G A intron_variant CLLE-ES 15 59384043 59384043 single base substitution C T downstream_gene_variant CLLE-ES 15 59384043 59384043 single base substitution C T intron_variant CLLE-ES 15 59384043 59384043 single base substitution C T upstream_gene_variant CLLE-ES 15 59387142 59387142 single base substitution T C 3_prime_UTR_variant CLLE-ES 15 59387142 59387142 single base substitution T C downstream_gene_variant CLLE-ES 15 59387142 59387142 single base substitution T C exon_variant COAD-US 15 59175945 59175945 single base substitution C T intron_variant COAD-US 15 59179213 59179213 single base substitution T C intron_variant COAD-US 15 59179261 59179261 single base substitution A C intron_variant COAD-US 15 59180631 59180631 single base substitution C T intron_variant COAD-US 15 59181649 59181649 single base substitution G A intron_variant COAD-US 15 59182525 59182526 deletion of <=200bp TC - intron_variant COAD-US 15 59185151 59185151 single base substitution A G intron_variant COAD-US 15 59189386 59189386 single base substitution A G intron_variant COAD-US 15 59191914 59191914 single base substitution A G intron_variant COAD-US 15 59209190 59209190 insertion of <=200bp - T intron_variant COAD-US 15 59323048 59323048 single base substitution C G missense_variant N32K 96C>G COAD-US 15 59323048 59323048 single base substitution C G missense_variant N9K 27C>G COAD-US 15 59323048 59323048 single base substitution C G upstream_gene_variant COAD-US 15 59323704 59323705 deletion of <=200bp AA - downstream_gene_variant COAD-US 15 59323704 59323705 deletion of <=200bp AA - frameshift_variant Q228 COAD-US 15 59323704 59323705 deletion of <=200bp AA - upstream_gene_variant COAD-US 15 59347929 59347929 single base substitution C A synonymous_variant S352S 1056C>A COAD-US 15 59347929 59347929 single base substitution C A synonymous_variant S85S 255C>A COAD-US 15 59368167 59368167 single base substitution G A synonymous_variant V567V 1701G>A COAD-US 15 59368167 59368167 single base substitution G A upstream_gene_variant COAD-US 15 59376343 59376343 deletion of <=200bp C - exon_variant COAD-US 15 59376343 59376343 deletion of <=200bp C - frameshift_variant R771 COAD-US 15 59376343 59376343 deletion of <=200bp C - frameshift_variant R780 COAD-US 15 59376343 59376343 deletion of <=200bp C - upstream_gene_variant COAD-US 15 59383297 59383297 single base substitution C T downstream_gene_variant COAD-US 15 59383297 59383297 single base substitution C T exon_variant COAD-US 15 59383297 59383297 single base substitution C T missense_variant R895C 2683C>T COAD-US 15 59383297 59383297 single base substitution C T missense_variant R904C 2710C>T COAD-US 15 59383297 59383297 single base substitution C T upstream_gene_variant COAD-US 15 59386986 59386986 single base substitution C A downstream_gene_variant COAD-US 15 59386986 59386986 single base substitution C A exon_variant COAD-US 15 59386986 59386986 single base substitution C A missense_variant L950I 2848C>A COAD-US 15 59386986 59386986 single base substitution C A missense_variant L958I 2872C>A COAD-US 15 59386986 59386986 single base substitution C A missense_variant L959I 2875C>A COAD-US 15 59386986 59386986 single base substitution C A missense_variant L967I 2899C>A COCA-CN 15 59179102 59179102 single base substitution A G intron_variant COCA-CN 15 59182464 59182464 single base substitution G T intron_variant COCA-CN 15 59182503 59182503 single base substitution T A intron_variant COCA-CN 15 59182565 59182565 single base substitution T G intron_variant COCA-CN 15 59185394 59185394 single base substitution C T intron_variant COCA-CN 15 59185972 59185972 single base substitution T G intron_variant COCA-CN 15 59189290 59189290 single base substitution G T intron_variant COCA-CN 15 59189331 59189331 single base substitution A C intron_variant COCA-CN 15 59191759 59191759 single base substitution C A intron_variant COCA-CN 15 59274509 59274509 single base substitution T C intron_variant COCA-CN 15 59296159 59296159 single base substitution C A intron_variant COCA-CN 15 59296172 59296172 single base substitution G T intron_variant COCA-CN 15 59323736 59323736 single base substitution C T downstream_gene_variant COCA-CN 15 59323736 59323736 single base substitution C T stop_gained R239* 715C>T COCA-CN 15 59323736 59323736 single base substitution C T upstream_gene_variant COCA-CN 15 59368510 59368510 single base substitution T G intron_variant COCA-CN 15 59368510 59368510 single base substitution T G upstream_gene_variant COCA-CN 15 59376531 59376531 single base substitution T C exon_variant COCA-CN 15 59376531 59376531 single base substitution T C intron_variant COCA-CN 15 59376531 59376531 single base substitution T C upstream_gene_variant EOPC-DE 15 59211665 59211665 single base substitution G A intron_variant EOPC-DE 15 59226203 59226203 single base substitution C T intron_variant EOPC-DE 15 59273885 59273885 single base substitution T A intron_variant EOPC-DE 15 59309590 59309590 single base substitution T C intron_variant EOPC-DE 15 59323724 59323724 single base substitution C T downstream_gene_variant EOPC-DE 15 59323724 59323724 single base substitution C T stop_gained Q235* 703C>T EOPC-DE 15 59323724 59323724 single base substitution C T upstream_gene_variant ESAD-UK 15 59153369 59153369 single base substitution G A upstream_gene_variant ESAD-UK 15 59155596 59155596 single base substitution G A upstream_gene_variant ESAD-UK 15 59156973 59156973 single base substitution C A upstream_gene_variant ESAD-UK 15 59160318 59160318 single base substitution C T intron_variant ESAD-UK 15 59163871 59163871 single base substitution A T intron_variant ESAD-UK 15 59164020 59164020 deletion of <=200bp A - intron_variant ESAD-UK 15 59165179 59165179 single base substitution T G intron_variant ESAD-UK 15 59165205 59165205 single base substitution T C intron_variant ESAD-UK 15 59169118 59169118 single base substitution A C intron_variant ESAD-UK 15 59172239 59172239 single base substitution C T intron_variant ESAD-UK 15 59185395 59185395 single base substitution G A intron_variant ESAD-UK 15 59186483 59186483 single base substitution G A intron_variant ESAD-UK 15 59188402 59188402 single base substitution C A intron_variant ESAD-UK 15 59188830 59188830 single base substitution T C intron_variant ESAD-UK 15 59190187 59190187 single base substitution C T intron_variant ESAD-UK 15 59195031 59195031 single base substitution T A intron_variant ESAD-UK 15 59196191 59196191 single base substitution C T intron_variant ESAD-UK 15 59198116 59198116 single base substitution C T intron_variant ESAD-UK 15 59198355 59198355 single base substitution T A intron_variant ESAD-UK 15 59200738 59200738 single base substitution A T intron_variant ESAD-UK 15 59209987 59209987 single base substitution C T intron_variant ESAD-UK 15 59212411 59212411 single base substitution G A intron_variant ESAD-UK 15 59212797 59212797 single base substitution G A intron_variant ESAD-UK 15 59215795 59215795 single base substitution C G intron_variant ESAD-UK 15 59216331 59216331 single base substitution G A intron_variant ESAD-UK 15 59219187 59219187 single base substitution G T intron_variant ESAD-UK 15 59223508 59223508 single base substitution G A intron_variant ESAD-UK 15 59224311 59224311 single base substitution T G intron_variant ESAD-UK 15 59224825 59224825 deletion of <=200bp A - intron_variant ESAD-UK 15 59227766 59227766 deletion of <=200bp T - intron_variant ESAD-UK 15 59233622 59233622 single base substitution T C intron_variant ESAD-UK 15 59235689 59235689 single base substitution G A intron_variant ESAD-UK 15 59236826 59236826 single base substitution G C intron_variant ESAD-UK 15 59238862 59238862 insertion of <=200bp - A intron_variant ESAD-UK 15 59239412 59239412 single base substitution A G intron_variant ESAD-UK 15 59247408 59247408 single base substitution A G intron_variant ESAD-UK 15 59249429 59249429 single base substitution G T intron_variant ESAD-UK 15 59250535 59250535 single base substitution A C intron_variant ESAD-UK 15 59250742 59250742 single base substitution A G intron_variant ESAD-UK 15 59252792 59252792 single base substitution C A intron_variant ESAD-UK 15 59255974 59255974 single base substitution C T intron_variant ESAD-UK 15 59259477 59259477 single base substitution G A intron_variant ESAD-UK 15 59259756 59259756 single base substitution C T intron_variant ESAD-UK 15 59261363 59261363 single base substitution T C intron_variant ESAD-UK 15 59262115 59262115 insertion of <=200bp - AAG intron_variant ESAD-UK 15 59266983 59266983 single base substitution G T intron_variant ESAD-UK 15 59267036 59267036 single base substitution T C intron_variant ESAD-UK 15 59270860 59270860 single base substitution A T intron_variant ESAD-UK 15 59272771 59272771 single base substitution A T intron_variant ESAD-UK 15 59273874 59273874 single base substitution G T intron_variant ESAD-UK 15 59276497 59276497 single base substitution G A intron_variant ESAD-UK 15 59276497 59276497 single base substitution G A upstream_gene_variant ESAD-UK 15 59276890 59276890 single base substitution T A intron_variant ESAD-UK 15 59276890 59276890 single base substitution T A upstream_gene_variant ESAD-UK 15 59277016 59277016 single base substitution C T intron_variant ESAD-UK 15 59277016 59277016 single base substitution C T upstream_gene_variant ESAD-UK 15 59279643 59279643 single base substitution A G intron_variant ESAD-UK 15 59279643 59279643 single base substitution A G upstream_gene_variant ESAD-UK 15 59285747 59285747 single base substitution A G intron_variant ESAD-UK 15 59287570 59287570 single base substitution A G intron_variant ESAD-UK 15 59289429 59289429 single base substitution C A intron_variant ESAD-UK 15 59290033 59290033 single base substitution C T intron_variant ESAD-UK 15 59293751 59293751 single base substitution G T intron_variant ESAD-UK 15 59298594 59298594 single base substitution C T intron_variant ESAD-UK 15 59298935 59298935 deletion of <=200bp A - intron_variant ESAD-UK 15 59299042 59299042 single base substitution A G intron_variant ESAD-UK 15 59300429 59300429 insertion of <=200bp - TTG intron_variant ESAD-UK 15 59300433 59300433 single base substitution G T intron_variant ESAD-UK 15 59300592 59300592 insertion of <=200bp - T intron_variant ESAD-UK 15 59300774 59300775 deletion of <=200bp AA - intron_variant ESAD-UK 15 59300776 59300776 single base substitution A T intron_variant ESAD-UK 15 59302784 59302784 single base substitution A T intron_variant ESAD-UK 15 59302785 59302785 single base substitution G A intron_variant ESAD-UK 15 59304289 59304289 single base substitution G A intron_variant ESAD-UK 15 59304816 59304816 single base substitution T A intron_variant ESAD-UK 15 59305384 59305384 deletion of <=200bp A - intron_variant ESAD-UK 15 59307260 59307260 single base substitution T A intron_variant ESAD-UK 15 59310899 59310899 single base substitution G T intron_variant ESAD-UK 15 59310915 59310915 single base substitution G A intron_variant ESAD-UK 15 59310931 59310931 single base substitution G A intron_variant ESAD-UK 15 59311023 59311023 deletion of <=200bp T - intron_variant ESAD-UK 15 59311448 59311448 single base substitution G A intron_variant ESAD-UK 15 59315985 59315985 deletion of <=200bp T - intron_variant ESAD-UK 15 59316838 59316838 single base substitution G T intron_variant ESAD-UK 15 59317033 59317033 single base substitution C T intron_variant ESAD-UK 15 59317412 59317412 single base substitution A C intron_variant ESAD-UK 15 59318495 59318495 insertion of <=200bp - G intron_variant ESAD-UK 15 59318495 59318495 insertion of <=200bp - G upstream_gene_variant ESAD-UK 15 59319738 59319738 single base substitution T C intron_variant ESAD-UK 15 59319738 59319738 single base substitution T C upstream_gene_variant ESAD-UK 15 59329699 59329699 single base substitution A T intron_variant ESAD-UK 15 59330815 59330815 deletion of <=200bp T - intron_variant ESAD-UK 15 59331110 59331110 deletion of <=200bp T - intron_variant ESAD-UK 15 59332688 59332688 single base substitution A T intron_variant ESAD-UK 15 59333315 59333315 single base substitution C A intron_variant ESAD-UK 15 59334841 59334841 single base substitution C A intron_variant ESAD-UK 15 59335107 59335107 single base substitution G A intron_variant ESAD-UK 15 59338678 59338678 single base substitution C G intron_variant ESAD-UK 15 59339190 59339190 single base substitution C T intron_variant ESAD-UK 15 59341828 59341828 single base substitution C T intron_variant ESAD-UK 15 59343750 59343750 single base substitution A G intron_variant ESAD-UK 15 59349650 59349650 single base substitution C G intron_variant ESAD-UK 15 59352916 59352916 single base substitution T A downstream_gene_variant ESAD-UK 15 59352916 59352916 single base substitution T A intron_variant ESAD-UK 15 59353010 59353010 single base substitution T A downstream_gene_variant ESAD-UK 15 59353010 59353010 single base substitution T A intron_variant ESAD-UK 15 59355331 59355331 single base substitution G A downstream_gene_variant ESAD-UK 15 59355331 59355331 single base substitution G A intron_variant ESAD-UK 15 59357105 59357105 single base substitution G A intron_variant ESAD-UK 15 59358346 59358346 single base substitution T G intron_variant ESAD-UK 15 59360008 59360008 single base substitution C G intron_variant ESAD-UK 15 59360496 59360496 deletion of <=200bp A - intron_variant ESAD-UK 15 59360510 59360510 insertion of <=200bp - A intron_variant ESAD-UK 15 59360594 59360594 single base substitution T C intron_variant ESAD-UK 15 59362081 59362081 single base substitution G A intron_variant ESAD-UK 15 59363901 59363901 single base substitution A T intron_variant ESAD-UK 15 59365088 59365088 single base substitution A C intron_variant ESAD-UK 15 59365691 59365691 single base substitution A T intron_variant ESAD-UK 15 59366315 59366315 single base substitution G A intron_variant ESAD-UK 15 59368259 59368259 single base substitution G A missense_variant R598Q 1793G>A ESAD-UK 15 59368259 59368259 single base substitution G A upstream_gene_variant ESAD-UK 15 59368689 59368689 single base substitution A G intron_variant ESAD-UK 15 59368689 59368689 single base substitution A G upstream_gene_variant ESAD-UK 15 59369727 59369727 single base substitution C T intron_variant ESAD-UK 15 59369727 59369727 single base substitution C T upstream_gene_variant ESAD-UK 15 59370014 59370014 single base substitution G T intron_variant ESAD-UK 15 59370014 59370014 single base substitution G T upstream_gene_variant ESAD-UK 15 59370833 59370833 single base substitution G A intron_variant ESAD-UK 15 59370833 59370833 single base substitution G A upstream_gene_variant ESAD-UK 15 59373359 59373359 single base substitution C G exon_variant ESAD-UK 15 59373359 59373359 single base substitution C G missense_variant P725A 2173C>G ESAD-UK 15 59373359 59373359 single base substitution C G upstream_gene_variant ESAD-UK 15 59373679 59373679 single base substitution G T intron_variant ESAD-UK 15 59373679 59373679 single base substitution G T upstream_gene_variant ESAD-UK 15 59373730 59373730 single base substitution C A intron_variant ESAD-UK 15 59373730 59373730 single base substitution C A upstream_gene_variant ESAD-UK 15 59373731 59373731 deletion of <=200bp A - intron_variant ESAD-UK 15 59373731 59373731 deletion of <=200bp A - upstream_gene_variant ESAD-UK 15 59376374 59376374 single base substitution A G exon_variant ESAD-UK 15 59376374 59376374 single base substitution A G missense_variant N782D 2344A>G ESAD-UK 15 59376374 59376374 single base substitution A G missense_variant N791D 2371A>G ESAD-UK 15 59376374 59376374 single base substitution A G upstream_gene_variant ESAD-UK 15 59376487 59376487 single base substitution C G exon_variant ESAD-UK 15 59376487 59376487 single base substitution C G intron_variant ESAD-UK 15 59376487 59376487 single base substitution C G upstream_gene_variant ESAD-UK 15 59378435 59378435 single base substitution C G downstream_gene_variant ESAD-UK 15 59378435 59378435 single base substitution C G intron_variant ESAD-UK 15 59379217 59379217 single base substitution C G downstream_gene_variant ESAD-UK 15 59379217 59379217 single base substitution C G intron_variant ESAD-UK 15 59382403 59382403 single base substitution G T downstream_gene_variant ESAD-UK 15 59382403 59382403 single base substitution G T intron_variant ESAD-UK 15 59382403 59382403 single base substitution G T upstream_gene_variant ESAD-UK 15 59383127 59383127 single base substitution A C downstream_gene_variant ESAD-UK 15 59383127 59383127 single base substitution A C intron_variant ESAD-UK 15 59383127 59383127 single base substitution A C upstream_gene_variant ESAD-UK 15 59387177 59387177 single base substitution T G 3_prime_UTR_variant ESAD-UK 15 59387177 59387177 single base substitution T G downstream_gene_variant ESAD-UK 15 59387177 59387177 single base substitution T G exon_variant ESAD-UK 15 59387292 59387292 insertion of <=200bp - T 3_prime_UTR_variant ESAD-UK 15 59387292 59387292 insertion of <=200bp - T downstream_gene_variant ESAD-UK 15 59387292 59387292 insertion of <=200bp - T exon_variant ESAD-UK 15 59387906 59387906 single base substitution A T 3_prime_UTR_variant ESAD-UK 15 59387906 59387906 single base substitution A T downstream_gene_variant ESAD-UK 15 59387906 59387906 single base substitution A T exon_variant ESAD-UK 15 59390710 59390710 single base substitution T G downstream_gene_variant ESAD-UK 15 59391754 59391754 single base substitution C T downstream_gene_variant ESAD-UK 15 59391893 59391893 single base substitution T G downstream_gene_variant ESCA-CN 15 59225515 59225524 deletion of <=200bp GGCAGCCGGA - intron_variant ESCA-CN 15 59368383 59368383 single base substitution C G synonymous_variant L639L 1917C>G ESCA-CN 15 59368383 59368383 single base substitution C G upstream_gene_variant GACA-CN 15 59373164 59373164 single base substitution C T exon_variant GACA-CN 15 59373164 59373164 single base substitution C T stop_gained Q660* 1978C>T GACA-CN 15 59373164 59373164 single base substitution C T upstream_gene_variant GBM-US 15 59181723 59181723 single base substitution G C intron_variant GBM-US 15 59186379 59186379 single base substitution G A intron_variant GBM-US 15 59323149 59323149 single base substitution T C missense_variant I43T 128T>C GBM-US 15 59323149 59323149 single base substitution T C missense_variant I66T 197T>C GBM-US 15 59323149 59323149 single base substitution T C upstream_gene_variant KIRC-US 15 59153166 59153166 insertion of <=200bp - A upstream_gene_variant KIRC-US 15 59205785 59205786 deletion of <=200bp TA - intron_variant KIRP-US 15 59344604 59344604 single base substitution G T missense_variant E327D 981G>T KIRP-US 15 59344604 59344604 single base substitution G T missense_variant E60D 180G>T LAML-KR 15 59241642 59241642 single base substitution G A intron_variant LAML-KR 15 59252599 59252599 single base substitution G A intron_variant LAML-KR 15 59278973 59278973 single base substitution C A intron_variant LAML-KR 15 59278973 59278973 single base substitution C A upstream_gene_variant LAML-KR 15 59335372 59335372 single base substitution G T intron_variant LAML-KR 15 59341646 59341646 single base substitution A G intron_variant LAML-KR 15 59376531 59376531 single base substitution T C exon_variant LAML-KR 15 59376531 59376531 single base substitution T C intron_variant LAML-KR 15 59376531 59376531 single base substitution T C upstream_gene_variant LGG-US 15 59182564 59182565 deletion of <=200bp CT - intron_variant LGG-US 15 59186365 59186365 single base substitution T C intron_variant LICA-CN 15 59175981 59175981 single base substitution T A intron_variant LICA-CN 15 59186066 59186066 single base substitution G A intron_variant LICA-FR 15 59186905 59186905 insertion of <=200bp - T intron_variant LICA-FR 15 59187825 59187825 single base substitution A T intron_variant LICA-FR 15 59197088 59197088 single base substitution T G intron_variant LICA-FR 15 59202943 59202943 deletion of <=200bp T - intron_variant LICA-FR 15 59208016 59208018 deletion of <=200bp ATG - intron_variant LICA-FR 15 59209198 59209198 single base substitution C T intron_variant LICA-FR 15 59217273 59217273 insertion of <=200bp - AA intron_variant LICA-FR 15 59218882 59218882 single base substitution C A intron_variant LICA-FR 15 59234299 59234299 single base substitution C A intron_variant LICA-FR 15 59251790 59251790 single base substitution G A intron_variant LICA-FR 15 59255281 59255281 single base substitution A G intron_variant LICA-FR 15 59261946 59261946 single base substitution T C intron_variant LICA-FR 15 59263242 59263242 single base substitution G T intron_variant LICA-FR 15 59305598 59305598 single base substitution C T intron_variant LICA-FR 15 59307162 59307162 single base substitution G A intron_variant LICA-FR 15 59309016 59309016 single base substitution A G intron_variant LICA-FR 15 59316239 59316239 single base substitution A G intron_variant LICA-FR 15 59345366 59345366 single base substitution T G intron_variant LICA-FR 15 59347941 59347941 single base substitution A T synonymous_variant A356A 1068A>T LICA-FR 15 59347941 59347941 single base substitution A T synonymous_variant A89A 267A>T LICA-FR 15 59358096 59358096 single base substitution G T intron_variant LICA-FR 15 59359142 59359142 insertion of <=200bp - CAC inframe_insertion H516HH LICA-FR 15 59367870 59367870 single base substitution A G intron_variant LICA-FR 15 59371881 59371881 single base substitution A T intron_variant LICA-FR 15 59371881 59371881 single base substitution A T upstream_gene_variant LICA-FR 15 59378753 59378753 single base substitution A G downstream_gene_variant LICA-FR 15 59378753 59378753 single base substitution A G intron_variant LICA-FR 15 59389027 59389027 single base substitution A T 3_prime_UTR_variant LICA-FR 15 59389027 59389027 single base substitution A T downstream_gene_variant LIHC-US 15 59192012 59192012 single base substitution A G intron_variant LIHC-US 15 59373264 59373264 single base substitution A G exon_variant LIHC-US 15 59373264 59373264 single base substitution A G missense_variant H693R 2078A>G LIHC-US 15 59373264 59373264 single base substitution A G upstream_gene_variant LINC-JP 15 59156269 59156269 single base substitution A T upstream_gene_variant LINC-JP 15 59167533 59167533 single base substitution C A intron_variant LINC-JP 15 59180826 59180826 single base substitution T C intron_variant LINC-JP 15 59181759 59181759 single base substitution G C intron_variant LINC-JP 15 59186039 59186039 single base substitution A G intron_variant LINC-JP 15 59187093 59187093 single base substitution A G intron_variant LINC-JP 15 59191834 59191834 single base substitution C T intron_variant LINC-JP 15 59191963 59191966 deletion of <=200bp GAGT - intron_variant LINC-JP 15 59207745 59207745 single base substitution T C intron_variant LINC-JP 15 59224479 59224479 single base substitution G C intron_variant LINC-JP 15 59228558 59228558 single base substitution A C intron_variant LINC-JP 15 59263800 59263800 single base substitution C T intron_variant LINC-JP 15 59264786 59264786 single base substitution T C intron_variant LINC-JP 15 59303226 59303226 single base substitution T A intron_variant LINC-JP 15 59303708 59303708 single base substitution A G intron_variant LINC-JP 15 59314065 59314065 single base substitution A T intron_variant LINC-JP 15 59316274 59316274 single base substitution C A intron_variant LINC-JP 15 59321576 59321576 single base substitution T G intron_variant LINC-JP 15 59321576 59321576 single base substitution T G upstream_gene_variant LINC-JP 15 59323271 59323271 single base substitution G T stop_gained E107* 319G>T LINC-JP 15 59323271 59323271 single base substitution G T stop_gained E84* 250G>T LINC-JP 15 59323271 59323271 single base substitution G T upstream_gene_variant LINC-JP 15 59323586 59323586 single base substitution A G downstream_gene_variant LINC-JP 15 59323586 59323586 single base substitution A G missense_variant T189A 565A>G LINC-JP 15 59323586 59323586 single base substitution A G upstream_gene_variant LINC-JP 15 59344765 59344765 single base substitution T G intron_variant LINC-JP 15 59350538 59350538 single base substitution C A intron_variant LINC-JP 15 59364780 59364780 single base substitution G A intron_variant LINC-JP 15 59367837 59367837 single base substitution T C intron_variant LINC-JP 15 59382243 59382243 single base substitution A G downstream_gene_variant LINC-JP 15 59382243 59382243 single base substitution A G intron_variant LINC-JP 15 59382243 59382243 single base substitution A G upstream_gene_variant LINC-JP 15 59383234 59383234 single base substitution A G downstream_gene_variant LINC-JP 15 59383234 59383234 single base substitution A G intron_variant LINC-JP 15 59383234 59383234 single base substitution A G upstream_gene_variant LINC-JP 15 59384677 59384677 single base substitution C G downstream_gene_variant LINC-JP 15 59384677 59384677 single base substitution C G intron_variant LINC-JP 15 59384677 59384677 single base substitution C G upstream_gene_variant LINC-JP 15 59384731 59384731 single base substitution C A downstream_gene_variant LINC-JP 15 59384731 59384731 single base substitution C A exon_variant LINC-JP 15 59384731 59384731 single base substitution C A splice_region_variant LINC-JP 15 59384731 59384731 single base substitution C A stop_gained S920* 2759C>A LINC-JP 15 59384731 59384731 single base substitution C A stop_gained S929* 2786C>A LINC-JP 15 59384731 59384731 single base substitution C A upstream_gene_variant LINC-JP 15 59384868 59384868 single base substitution A T downstream_gene_variant LINC-JP 15 59384868 59384868 single base substitution A T intron_variant LINC-JP 15 59384868 59384868 single base substitution A T upstream_gene_variant LIRI-JP 15 59155154 59155154 single base substitution T C upstream_gene_variant LIRI-JP 15 59157009 59157009 single base substitution G C upstream_gene_variant LIRI-JP 15 59157010 59157010 single base substitution G T upstream_gene_variant LIRI-JP 15 59158646 59158646 single base substitution G A intron_variant LIRI-JP 15 59162225 59162225 single base substitution T G intron_variant LIRI-JP 15 59166320 59166320 single base substitution T C intron_variant LIRI-JP 15 59166461 59166461 single base substitution T C intron_variant LIRI-JP 15 59167497 59167497 single base substitution T C intron_variant LIRI-JP 15 59170749 59170749 single base substitution A C intron_variant LIRI-JP 15 59171138 59171156 deletion of <=200bp AGACCAAAAGAATGCCTTT - intron_variant LIRI-JP 15 59171392 59171392 single base substitution T C intron_variant LIRI-JP 15 59171999 59171999 single base substitution T C intron_variant LIRI-JP 15 59172153 59172153 single base substitution G T intron_variant LIRI-JP 15 59172164 59172164 single base substitution A G intron_variant LIRI-JP 15 59172966 59172966 single base substitution T C intron_variant LIRI-JP 15 59174266 59174266 single base substitution C T intron_variant LIRI-JP 15 59176810 59176810 single base substitution C A intron_variant LIRI-JP 15 59178912 59178912 single base substitution T G intron_variant LIRI-JP 15 59179702 59179702 single base substitution C A intron_variant LIRI-JP 15 59181846 59181852 deletion of <=200bp AACCATC - intron_variant LIRI-JP 15 59185474 59185474 single base substitution T C intron_variant LIRI-JP 15 59185489 59185489 single base substitution T A intron_variant LIRI-JP 15 59186284 59186284 single base substitution C A intron_variant LIRI-JP 15 59187564 59187564 single base substitution T G intron_variant LIRI-JP 15 59188299 59188299 single base substitution G T intron_variant LIRI-JP 15 59189109 59189109 single base substitution A G intron_variant LIRI-JP 15 59189899 59189899 single base substitution T C intron_variant LIRI-JP 15 59190145 59190145 single base substitution T C intron_variant LIRI-JP 15 59190812 59190812 single base substitution A G intron_variant LIRI-JP 15 59190813 59190813 single base substitution C T intron_variant LIRI-JP 15 59191323 59191323 single base substitution T C intron_variant LIRI-JP 15 59191639 59191639 single base substitution T C intron_variant LIRI-JP 15 59192885 59192885 single base substitution T C intron_variant LIRI-JP 15 59192926 59192926 single base substitution C A intron_variant LIRI-JP 15 59193072 59193072 single base substitution G A intron_variant LIRI-JP 15 59196932 59196932 single base substitution C A intron_variant LIRI-JP 15 59198077 59198077 single base substitution T G intron_variant LIRI-JP 15 59198708 59198708 single base substitution T C intron_variant LIRI-JP 15 59199982 59199982 single base substitution T C intron_variant LIRI-JP 15 59200039 59200039 single base substitution A C intron_variant LIRI-JP 15 59200504 59200504 single base substitution C T intron_variant LIRI-JP 15 59201770 59201770 single base substitution A T intron_variant LIRI-JP 15 59203502 59203502 single base substitution T C intron_variant LIRI-JP 15 59203866 59203866 single base substitution T A intron_variant LIRI-JP 15 59204088 59204088 single base substitution A C intron_variant LIRI-JP 15 59206029 59206029 single base substitution T G intron_variant LIRI-JP 15 59209570 59209571 deletion of <=200bp TC - intron_variant LIRI-JP 15 59210470 59210470 single base substitution T C intron_variant LIRI-JP 15 59210964 59210964 single base substitution C T intron_variant LIRI-JP 15 59211273 59211273 single base substitution G A intron_variant LIRI-JP 15 59213314 59213314 single base substitution G A intron_variant LIRI-JP 15 59214964 59214964 single base substitution T C intron_variant LIRI-JP 15 59218728 59218728 single base substitution A C intron_variant LIRI-JP 15 59219365 59219365 single base substitution A G intron_variant LIRI-JP 15 59220321 59220321 single base substitution T C intron_variant LIRI-JP 15 59222698 59222698 single base substitution A C intron_variant LIRI-JP 15 59222713 59222713 single base substitution A C intron_variant LIRI-JP 15 59223888 59223888 single base substitution T C intron_variant LIRI-JP 15 59228408 59228408 single base substitution A C intron_variant LIRI-JP 15 59229754 59229754 single base substitution G A intron_variant LIRI-JP 15 59229908 59229908 single base substitution G A intron_variant LIRI-JP 15 59231233 59231233 single base substitution C T intron_variant LIRI-JP 15 59232449 59232449 single base substitution A T intron_variant LIRI-JP 15 59234358 59234358 single base substitution A G intron_variant LIRI-JP 15 59236083 59236083 single base substitution A G intron_variant LIRI-JP 15 59236116 59236116 single base substitution A G intron_variant LIRI-JP 15 59236215 59236215 single base substitution A G intron_variant LIRI-JP 15 59236922 59236922 single base substitution T C intron_variant LIRI-JP 15 59239175 59239178 deletion of <=200bp ACAG - intron_variant LIRI-JP 15 59239912 59239912 single base substitution C T intron_variant LIRI-JP 15 59241659 59241659 single base substitution G A intron_variant LIRI-JP 15 59241711 59241711 single base substitution A G intron_variant LIRI-JP 15 59245813 59245813 single base substitution C T intron_variant LIRI-JP 15 59251509 59251509 single base substitution C A intron_variant LIRI-JP 15 59254079 59254079 single base substitution G A intron_variant LIRI-JP 15 59256121 59256121 single base substitution G A intron_variant LIRI-JP 15 59257196 59257196 single base substitution G T intron_variant LIRI-JP 15 59258702 59258702 single base substitution T C intron_variant LIRI-JP 15 59262780 59262780 single base substitution C T intron_variant LIRI-JP 15 59263535 59263535 single base substitution G T intron_variant LIRI-JP 15 59263795 59263795 single base substitution T C intron_variant LIRI-JP 15 59264640 59264640 single base substitution C T intron_variant LIRI-JP 15 59265071 59265071 single base substitution G A intron_variant LIRI-JP 15 59265469 59265469 single base substitution C A intron_variant LIRI-JP 15 59271946 59271946 single base substitution A G intron_variant LIRI-JP 15 59277063 59277063 single base substitution C T intron_variant LIRI-JP 15 59277063 59277063 single base substitution C T upstream_gene_variant LIRI-JP 15 59277310 59277310 deletion of <=200bp C - intron_variant LIRI-JP 15 59277310 59277310 deletion of <=200bp C - upstream_gene_variant LIRI-JP 15 59277681 59277681 single base substitution C T intron_variant LIRI-JP 15 59277681 59277681 single base substitution C T upstream_gene_variant LIRI-JP 15 59279039 59279039 single base substitution C T intron_variant LIRI-JP 15 59279039 59279039 single base substitution C T upstream_gene_variant LIRI-JP 15 59281321 59281321 single base substitution A T intron_variant LIRI-JP 15 59282111 59282111 single base substitution A G intron_variant LIRI-JP 15 59285646 59285646 single base substitution A C intron_variant LIRI-JP 15 59285743 59285743 single base substitution T C intron_variant LIRI-JP 15 59285783 59285783 single base substitution T A intron_variant LIRI-JP 15 59288459 59288470 deletion of <=200bp TAAGAAACTTTA - intron_variant LIRI-JP 15 59289057 59289057 single base substitution A G intron_variant LIRI-JP 15 59290491 59290491 single base substitution G C intron_variant LIRI-JP 15 59290931 59290931 single base substitution A T intron_variant LIRI-JP 15 59291458 59291458 single base substitution G A intron_variant LIRI-JP 15 59293902 59293902 single base substitution G A intron_variant LIRI-JP 15 59295333 59295333 single base substitution G A intron_variant LIRI-JP 15 59298006 59298006 single base substitution A G intron_variant LIRI-JP 15 59301782 59301782 single base substitution A G intron_variant LIRI-JP 15 59303257 59303257 single base substitution A G intron_variant LIRI-JP 15 59303953 59303953 single base substitution C G intron_variant LIRI-JP 15 59305420 59305420 single base substitution A G intron_variant LIRI-JP 15 59306605 59306605 single base substitution G T intron_variant LIRI-JP 15 59309736 59309736 single base substitution A G intron_variant LIRI-JP 15 59312402 59312402 single base substitution A T intron_variant LIRI-JP 15 59312632 59312632 single base substitution A G intron_variant LIRI-JP 15 59312744 59312744 single base substitution A G intron_variant LIRI-JP 15 59314287 59314287 single base substitution G C intron_variant LIRI-JP 15 59314560 59314560 single base substitution A G intron_variant LIRI-JP 15 59314639 59314639 single base substitution A G intron_variant LIRI-JP 15 59314673 59314673 single base substitution C T intron_variant LIRI-JP 15 59314713 59314713 single base substitution C T intron_variant LIRI-JP 15 59317996 59317996 single base substitution C T intron_variant LIRI-JP 15 59319201 59319201 single base substitution A G intron_variant LIRI-JP 15 59319201 59319201 single base substitution A G upstream_gene_variant LIRI-JP 15 59320431 59320431 single base substitution A G intron_variant LIRI-JP 15 59320431 59320431 single base substitution A G upstream_gene_variant LIRI-JP 15 59321198 59321198 single base substitution C T intron_variant LIRI-JP 15 59321198 59321198 single base substitution C T upstream_gene_variant LIRI-JP 15 59322323 59322323 single base substitution T A intron_variant LIRI-JP 15 59322323 59322323 single base substitution T A upstream_gene_variant LIRI-JP 15 59322523 59322523 single base substitution A G intron_variant LIRI-JP 15 59322523 59322523 single base substitution A G upstream_gene_variant LIRI-JP 15 59322680 59322680 single base substitution T C intron_variant LIRI-JP 15 59322680 59322680 single base substitution T C upstream_gene_variant LIRI-JP 15 59323496 59323512 deletion of <=200bp AAAGAAGTCTCTGTAAG - downstream_gene_variant LIRI-JP 15 59323496 59323512 deletion of <=200bp AAAGAAGTCTCTGTAAG - frameshift_variant KEVSVR159 LIRI-JP 15 59323496 59323512 deletion of <=200bp AAAGAAGTCTCTGTAAG - upstream_gene_variant LIRI-JP 15 59325336 59325336 insertion of <=200bp - GCTA downstream_gene_variant LIRI-JP 15 59325336 59325336 insertion of <=200bp - GCTA intron_variant LIRI-JP 15 59325972 59325972 single base substitution G A downstream_gene_variant LIRI-JP 15 59325972 59325972 single base substitution G A intron_variant LIRI-JP 15 59327422 59327422 single base substitution A G downstream_gene_variant LIRI-JP 15 59327422 59327422 single base substitution A G intron_variant LIRI-JP 15 59327948 59327948 single base substitution C T downstream_gene_variant LIRI-JP 15 59327948 59327948 single base substitution C T intron_variant LIRI-JP 15 59328361 59328361 single base substitution G A downstream_gene_variant LIRI-JP 15 59328361 59328361 single base substitution G A intron_variant LIRI-JP 15 59329795 59329795 single base substitution G A intron_variant LIRI-JP 15 59334684 59334684 single base substitution A G intron_variant LIRI-JP 15 59337591 59337591 single base substitution T C intron_variant LIRI-JP 15 59338208 59338208 single base substitution T C intron_variant LIRI-JP 15 59339125 59339125 single base substitution G A intron_variant LIRI-JP 15 59339961 59339961 single base substitution G T intron_variant LIRI-JP 15 59340813 59340813 single base substitution T A intron_variant LIRI-JP 15 59340924 59340924 single base substitution A T intron_variant LIRI-JP 15 59342445 59342445 single base substitution G T intron_variant LIRI-JP 15 59342547 59342547 single base substitution A G intron_variant LIRI-JP 15 59344182 59344182 single base substitution A G intron_variant LIRI-JP 15 59344847 59344847 single base substitution A C intron_variant LIRI-JP 15 59348397 59348397 single base substitution A G intron_variant LIRI-JP 15 59349644 59349644 single base substitution G T intron_variant LIRI-JP 15 59350893 59350893 single base substitution T G downstream_gene_variant LIRI-JP 15 59350893 59350893 single base substitution T G intron_variant LIRI-JP 15 59352165 59352165 single base substitution A G downstream_gene_variant LIRI-JP 15 59352165 59352165 single base substitution A G intron_variant LIRI-JP 15 59353999 59353999 single base substitution A G downstream_gene_variant LIRI-JP 15 59353999 59353999 single base substitution A G intron_variant LIRI-JP 15 59356098 59356098 single base substitution T G intron_variant LIRI-JP 15 59357791 59357791 single base substitution T G intron_variant LIRI-JP 15 59358764 59358764 single base substitution C T intron_variant LIRI-JP 15 59360296 59360296 single base substitution C G intron_variant LIRI-JP 15 59360604 59360604 single base substitution A G intron_variant LIRI-JP 15 59361643 59361643 single base substitution A G intron_variant LIRI-JP 15 59363195 59363195 single base substitution A T intron_variant LIRI-JP 15 59363823 59363823 single base substitution G T intron_variant LIRI-JP 15 59364812 59364812 single base substitution G A intron_variant LIRI-JP 15 59365286 59365286 single base substitution T A intron_variant LIRI-JP 15 59365287 59365287 single base substitution G T intron_variant LIRI-JP 15 59365623 59365623 single base substitution T C intron_variant LIRI-JP 15 59366080 59366080 single base substitution A G intron_variant LIRI-JP 15 59368205 59368205 single base substitution G A missense_variant G580D 1739G>A LIRI-JP 15 59368205 59368205 single base substitution G A upstream_gene_variant LIRI-JP 15 59368788 59368788 single base substitution A G intron_variant LIRI-JP 15 59368788 59368788 single base substitution A G upstream_gene_variant LIRI-JP 15 59369606 59369606 single base substitution C G intron_variant LIRI-JP 15 59369606 59369606 single base substitution C G upstream_gene_variant LIRI-JP 15 59369863 59369863 single base substitution A G intron_variant LIRI-JP 15 59369863 59369863 single base substitution A G upstream_gene_variant LIRI-JP 15 59372998 59373024 deletion of <=200bp CTTGAATACTTTACTTGATAAAGTATT - intron_variant LIRI-JP 15 59372998 59373024 deletion of <=200bp CTTGAATACTTTACTTGATAAAGTATT - upstream_gene_variant LIRI-JP 15 59373345 59373345 deletion of <=200bp T - exon_variant LIRI-JP 15 59373345 59373345 deletion of <=200bp T - frameshift_variant I720 LIRI-JP 15 59373345 59373345 deletion of <=200bp T - upstream_gene_variant LIRI-JP 15 59376852 59376852 single base substitution A G downstream_gene_variant LIRI-JP 15 59376852 59376852 single base substitution A G intron_variant LIRI-JP 15 59376852 59376852 single base substitution A G upstream_gene_variant LIRI-JP 15 59378606 59378606 single base substitution G A downstream_gene_variant LIRI-JP 15 59378606 59378606 single base substitution G A intron_variant LIRI-JP 15 59380365 59380365 single base substitution G C downstream_gene_variant LIRI-JP 15 59380365 59380365 single base substitution G C intron_variant LIRI-JP 15 59380948 59380948 single base substitution T C downstream_gene_variant LIRI-JP 15 59380948 59380948 single base substitution T C intron_variant LIRI-JP 15 59380948 59380948 single base substitution T C upstream_gene_variant LIRI-JP 15 59381564 59381566 deletion of <=200bp TTG - intron_variant LIRI-JP 15 59381564 59381566 deletion of <=200bp TTG - upstream_gene_variant LIRI-JP 15 59383301 59383301 single base substitution G A downstream_gene_variant LIRI-JP 15 59383301 59383301 single base substitution G A exon_variant LIRI-JP 15 59383301 59383301 single base substitution G A missense_variant G896E 2687G>A LIRI-JP 15 59383301 59383301 single base substitution G A missense_variant G905E 2714G>A LIRI-JP 15 59383301 59383301 single base substitution G A upstream_gene_variant LIRI-JP 15 59384511 59384511 single base substitution T G downstream_gene_variant LIRI-JP 15 59384511 59384511 single base substitution T G intron_variant LIRI-JP 15 59384511 59384511 single base substitution T G upstream_gene_variant LIRI-JP 15 59385722 59385722 single base substitution A G downstream_gene_variant LIRI-JP 15 59385722 59385722 single base substitution A G intron_variant LIRI-JP 15 59388225 59388225 single base substitution A T 3_prime_UTR_variant LIRI-JP 15 59388225 59388225 single base substitution A T downstream_gene_variant LIRI-JP 15 59388225 59388225 single base substitution A T exon_variant LIRI-JP 15 59391049 59391049 single base substitution T G downstream_gene_variant LIRI-JP 15 59394451 59394451 single base substitution A G downstream_gene_variant LUSC-KR 15 59158183 59158183 single base substitution G T intron_variant LUSC-KR 15 59164089 59164089 single base substitution C A intron_variant LUSC-KR 15 59164471 59164471 single base substitution A T intron_variant LUSC-KR 15 59166737 59166737 single base substitution C T intron_variant LUSC-KR 15 59178212 59178212 single base substitution G A intron_variant LUSC-KR 15 59183688 59183688 single base substitution T C intron_variant LUSC-KR 15 59192958 59192958 single base substitution C A intron_variant LUSC-KR 15 59205325 59205325 single base substitution G A intron_variant LUSC-KR 15 59219760 59219760 single base substitution C A intron_variant LUSC-KR 15 59227951 59227951 single base substitution G A intron_variant LUSC-KR 15 59228656 59228656 single base substitution G A intron_variant LUSC-KR 15 59228813 59228813 single base substitution G C intron_variant LUSC-KR 15 59240825 59240825 single base substitution A G intron_variant LUSC-KR 15 59241591 59241591 single base substitution G A intron_variant LUSC-KR 15 59242503 59242503 single base substitution A G intron_variant LUSC-KR 15 59247604 59247604 single base substitution T A intron_variant LUSC-KR 15 59248284 59248284 single base substitution G C intron_variant LUSC-KR 15 59254670 59254670 single base substitution G C intron_variant LUSC-KR 15 59255629 59255629 single base substitution C T intron_variant LUSC-KR 15 59256373 59256373 single base substitution G T intron_variant LUSC-KR 15 59257022 59257022 single base substitution G T intron_variant LUSC-KR 15 59259582 59259582 single base substitution G T intron_variant LUSC-KR 15 59274462 59274462 single base substitution T A intron_variant LUSC-KR 15 59274486 59274486 single base substitution T A intron_variant LUSC-KR 15 59274527 59274527 single base substitution T C intron_variant LUSC-KR 15 59277458 59277458 single base substitution C G intron_variant LUSC-KR 15 59277458 59277458 single base substitution C G upstream_gene_variant LUSC-KR 15 59287057 59287057 single base substitution G C intron_variant LUSC-KR 15 59287707 59287707 single base substitution G A intron_variant LUSC-KR 15 59294470 59294470 single base substitution C G intron_variant LUSC-KR 15 59296613 59296613 single base substitution T C intron_variant LUSC-KR 15 59300273 59300273 single base substitution A G intron_variant LUSC-KR 15 59301694 59301694 single base substitution C T intron_variant LUSC-KR 15 59301875 59301875 single base substitution C T intron_variant LUSC-KR 15 59305908 59305908 single base substitution A C intron_variant LUSC-KR 15 59306453 59306453 single base substitution C A intron_variant LUSC-KR 15 59306981 59306981 single base substitution G T intron_variant LUSC-KR 15 59323048 59323048 single base substitution C G missense_variant N32K 96C>G LUSC-KR 15 59323048 59323048 single base substitution C G missense_variant N9K 27C>G LUSC-KR 15 59323048 59323048 single base substitution C G upstream_gene_variant LUSC-KR 15 59337684 59337684 single base substitution G T intron_variant LUSC-KR 15 59339255 59339255 single base substitution C G intron_variant LUSC-KR 15 59339691 59339691 single base substitution C G intron_variant LUSC-KR 15 59353376 59353376 single base substitution A G downstream_gene_variant LUSC-KR 15 59353376 59353376 single base substitution A G intron_variant LUSC-KR 15 59356117 59356117 single base substitution C G intron_variant LUSC-KR 15 59358280 59358280 single base substitution C T intron_variant LUSC-KR 15 59359425 59359425 single base substitution G C intron_variant LUSC-KR 15 59360060 59360060 single base substitution C T intron_variant LUSC-KR 15 59361041 59361041 single base substitution C T intron_variant LUSC-KR 15 59362512 59362512 single base substitution C G intron_variant LUSC-KR 15 59366763 59366763 single base substitution C G intron_variant LUSC-KR 15 59367794 59367794 single base substitution G A intron_variant LUSC-KR 15 59373145 59373145 single base substitution G C exon_variant LUSC-KR 15 59373145 59373145 single base substitution G C missense_variant L653F 1959G>C LUSC-KR 15 59373145 59373145 single base substitution G C upstream_gene_variant LUSC-KR 15 59377162 59377162 single base substitution C G downstream_gene_variant LUSC-KR 15 59377162 59377162 single base substitution C G intron_variant LUSC-KR 15 59377162 59377162 single base substitution C G upstream_gene_variant LUSC-KR 15 59383839 59383839 single base substitution C T downstream_gene_variant LUSC-KR 15 59383839 59383839 single base substitution C T intron_variant LUSC-KR 15 59383839 59383839 single base substitution C T upstream_gene_variant LUSC-KR 15 59385560 59385560 single base substitution T C downstream_gene_variant LUSC-KR 15 59385560 59385560 single base substitution T C intron_variant LUSC-KR 15 59385560 59385560 single base substitution T C upstream_gene_variant LUSC-KR 15 59385852 59385852 single base substitution A C downstream_gene_variant LUSC-KR 15 59385852 59385852 single base substitution A C intron_variant LUSC-KR 15 59385988 59385988 single base substitution C T downstream_gene_variant LUSC-KR 15 59385988 59385988 single base substitution C T intron_variant LUSC-KR 15 59393281 59393281 single base substitution A T downstream_gene_variant LUSC-US 15 59179632 59179632 single base substitution C G intron_variant LUSC-US 15 59191709 59191709 single base substitution C T intron_variant LUSC-US 15 59224582 59224582 single base substitution G C intron_variant LUSC-US 15 59224609 59224609 single base substitution T C intron_variant LUSC-US 15 59225621 59225621 single base substitution G C intron_variant LUSC-US 15 59323142 59323142 single base substitution G C missense_variant E41Q 121G>C LUSC-US 15 59323142 59323142 single base substitution G C missense_variant E64Q 190G>C LUSC-US 15 59323142 59323142 single base substitution G C upstream_gene_variant LUSC-US 15 59323210 59323210 single base substitution A C missense_variant E63D 189A>C LUSC-US 15 59323210 59323210 single base substitution A C missense_variant E86D 258A>C LUSC-US 15 59323210 59323210 single base substitution A C upstream_gene_variant LUSC-US 15 59344503 59344503 single base substitution G A splice_acceptor_variant LUSC-US 15 59373224 59373224 single base substitution C G exon_variant LUSC-US 15 59373224 59373224 single base substitution C G missense_variant Q680E 2038C>G LUSC-US 15 59373224 59373224 single base substitution C G upstream_gene_variant LUSC-US 15 59373363 59373363 single base substitution C T exon_variant LUSC-US 15 59373363 59373363 single base substitution C T missense_variant P726L 2177C>T LUSC-US 15 59373363 59373363 single base substitution C T upstream_gene_variant LUSC-US 15 59377922 59377922 single base substitution T C downstream_gene_variant LUSC-US 15 59377922 59377922 single base substitution T C exon_variant LUSC-US 15 59377922 59377922 single base substitution T C synonymous_variant L830L 2488T>C LUSC-US 15 59377922 59377922 single base substitution T C synonymous_variant L839L 2515T>C MALY-DE 15 59171971 59171971 single base substitution C T intron_variant MALY-DE 15 59179709 59179709 single base substitution C T intron_variant MALY-DE 15 59209982 59209982 single base substitution T G intron_variant MALY-DE 15 59211127 59211127 single base substitution T A intron_variant MALY-DE 15 59216614 59216614 single base substitution A T intron_variant MALY-DE 15 59216633 59216633 single base substitution A G intron_variant MALY-DE 15 59216635 59216635 single base substitution T A intron_variant MALY-DE 15 59216642 59216642 single base substitution T C intron_variant MALY-DE 15 59225721 59225721 single base substitution C A intron_variant MALY-DE 15 59225732 59225732 single base substitution C A intron_variant MALY-DE 15 59232210 59232210 single base substitution C T intron_variant MALY-DE 15 59234551 59234551 single base substitution G T intron_variant MALY-DE 15 59235378 59235378 single base substitution T C intron_variant MALY-DE 15 59236021 59236021 single base substitution G A intron_variant MALY-DE 15 59236382 59236382 insertion of <=200bp - T intron_variant MALY-DE 15 59237223 59237223 single base substitution T G intron_variant MALY-DE 15 59238718 59238718 single base substitution A C intron_variant MALY-DE 15 59240452 59240467 deletion of <=200bp GGTCAAAATGGAAAGC - intron_variant MALY-DE 15 59241424 59241424 single base substitution G A intron_variant MALY-DE 15 59249882 59249882 insertion of <=200bp - GA intron_variant MALY-DE 15 59249882 59249883 deletion of <=200bp GA - intron_variant MALY-DE 15 59252133 59252133 deletion of <=200bp T - intron_variant MALY-DE 15 59256203 59256203 single base substitution T C intron_variant MALY-DE 15 59257066 59257066 single base substitution G A intron_variant MALY-DE 15 59259428 59259428 single base substitution T G intron_variant MALY-DE 15 59259662 59259662 single base substitution T C intron_variant MALY-DE 15 59260128 59260128 single base substitution T A intron_variant MALY-DE 15 59264137 59264137 deletion of <=200bp T - intron_variant MALY-DE 15 59273223 59273223 single base substitution G A intron_variant MALY-DE 15 59276889 59276889 single base substitution T A intron_variant MALY-DE 15 59276889 59276889 single base substitution T A upstream_gene_variant MALY-DE 15 59277323 59277323 single base substitution A G intron_variant MALY-DE 15 59277323 59277323 single base substitution A G upstream_gene_variant MALY-DE 15 59279321 59279321 single base substitution C T intron_variant MALY-DE 15 59279321 59279321 single base substitution C T upstream_gene_variant MALY-DE 15 59281432 59281432 single base substitution C G intron_variant MALY-DE 15 59288798 59288798 single base substitution A G intron_variant MALY-DE 15 59294263 59294263 single base substitution C G intron_variant MALY-DE 15 59297301 59297301 single base substitution A G intron_variant MALY-DE 15 59297871 59297871 insertion of <=200bp - A intron_variant MALY-DE 15 59299180 59299180 single base substitution T C intron_variant MALY-DE 15 59299806 59299806 single base substitution C A intron_variant MALY-DE 15 59303976 59303976 single base substitution A C intron_variant MALY-DE 15 59311660 59311660 single base substitution G C intron_variant MALY-DE 15 59315212 59315212 single base substitution G A intron_variant MALY-DE 15 59318117 59318117 single base substitution C T intron_variant MALY-DE 15 59318117 59318117 single base substitution C T upstream_gene_variant MALY-DE 15 59326388 59326388 single base substitution T G downstream_gene_variant MALY-DE 15 59326388 59326388 single base substitution T G intron_variant MALY-DE 15 59343627 59343627 single base substitution A T intron_variant MALY-DE 15 59343971 59343971 insertion of <=200bp - AATA intron_variant MALY-DE 15 59343971 59343982 deletion of <=200bp AATAAATAAATA - intron_variant MALY-DE 15 59344677 59344677 single base substitution T C intron_variant MALY-DE 15 59350256 59350256 single base substitution T A intron_variant MALY-DE 15 59350352 59350352 single base substitution T A intron_variant MALY-DE 15 59351560 59351560 single base substitution G A downstream_gene_variant MALY-DE 15 59351560 59351560 single base substitution G A intron_variant MALY-DE 15 59365371 59365371 single base substitution C G intron_variant MALY-DE 15 59365732 59365732 single base substitution A C intron_variant MALY-DE 15 59374127 59374127 single base substitution G A intron_variant MALY-DE 15 59374127 59374127 single base substitution G A upstream_gene_variant MALY-DE 15 59374128 59374128 single base substitution A G intron_variant MALY-DE 15 59374128 59374128 single base substitution A G upstream_gene_variant MALY-DE 15 59382014 59382014 insertion of <=200bp - TA downstream_gene_variant MALY-DE 15 59382014 59382014 insertion of <=200bp - TA intron_variant MALY-DE 15 59382014 59382014 insertion of <=200bp - TA upstream_gene_variant MALY-DE 15 59390247 59390248 deletion of <=200bp AC - downstream_gene_variant MALY-DE 15 59392977 59392977 single base substitution A T downstream_gene_variant MALY-DE 15 59393001 59393001 single base substitution A T downstream_gene_variant MELA-AU 15 59152890 59152890 single base substitution A C upstream_gene_variant MELA-AU 15 59154035 59154035 single base substitution A G upstream_gene_variant MELA-AU 15 59154125 59154125 single base substitution C T upstream_gene_variant MELA-AU 15 59155259 59155259 single base substitution T G upstream_gene_variant MELA-AU 15 59155601 59155601 single base substitution G A upstream_gene_variant MELA-AU 15 59155820 59155820 single base substitution C T upstream_gene_variant MELA-AU 15 59156088 59156088 single base substitution T A upstream_gene_variant MELA-AU 15 59156378 59156378 single base substitution C T upstream_gene_variant MELA-AU 15 59157273 59157273 single base substitution C T upstream_gene_variant MELA-AU 15 59157550 59157550 single base substitution G A intron_variant MELA-AU 15 59157697 59157697 single base substitution G A intron_variant MELA-AU 15 59157930 59157930 single base substitution G A intron_variant MELA-AU 15 59158532 59158532 single base substitution C T intron_variant MELA-AU 15 59158993 59158993 single base substitution G A intron_variant MELA-AU 15 59159048 59159048 single base substitution G A intron_variant MELA-AU 15 59160114 59160114 single base substitution C T intron_variant MELA-AU 15 59160310 59160311 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59161171 59161171 single base substitution C T intron_variant MELA-AU 15 59161721 59161721 single base substitution G A intron_variant MELA-AU 15 59162208 59162208 single base substitution G T intron_variant MELA-AU 15 59162597 59162597 single base substitution G A intron_variant MELA-AU 15 59162646 59162646 single base substitution G A intron_variant MELA-AU 15 59162859 59162859 single base substitution A G intron_variant MELA-AU 15 59163127 59163127 single base substitution C T intron_variant MELA-AU 15 59165511 59165511 single base substitution C G intron_variant MELA-AU 15 59165844 59165845 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59166375 59166375 single base substitution G A intron_variant MELA-AU 15 59169567 59169567 single base substitution G A intron_variant MELA-AU 15 59172342 59172342 single base substitution C G intron_variant MELA-AU 15 59173120 59173120 single base substitution A G intron_variant MELA-AU 15 59173153 59173153 single base substitution G A intron_variant MELA-AU 15 59173619 59173619 single base substitution G A intron_variant MELA-AU 15 59174386 59174386 insertion of <=200bp - AAAAAAAAAAAAC intron_variant MELA-AU 15 59174760 59174760 single base substitution G A intron_variant MELA-AU 15 59175542 59175542 single base substitution G A intron_variant MELA-AU 15 59175764 59175764 single base substitution C T intron_variant MELA-AU 15 59176065 59176065 single base substitution G A intron_variant MELA-AU 15 59177610 59177610 single base substitution G A intron_variant MELA-AU 15 59178015 59178015 single base substitution A G intron_variant MELA-AU 15 59178264 59178264 single base substitution A T intron_variant MELA-AU 15 59178657 59178657 single base substitution G A intron_variant MELA-AU 15 59179073 59179073 single base substitution T C intron_variant MELA-AU 15 59179238 59179238 single base substitution G A intron_variant MELA-AU 15 59179601 59179601 single base substitution A T intron_variant MELA-AU 15 59180636 59180636 single base substitution C T intron_variant MELA-AU 15 59181781 59181781 single base substitution A G intron_variant MELA-AU 15 59182050 59182050 single base substitution T G intron_variant MELA-AU 15 59182430 59182430 single base substitution G A intron_variant MELA-AU 15 59185256 59185256 single base substitution G A intron_variant MELA-AU 15 59185570 59185570 single base substitution G A intron_variant MELA-AU 15 59185996 59185996 single base substitution G A intron_variant MELA-AU 15 59185997 59185997 single base substitution G A intron_variant MELA-AU 15 59186996 59186996 single base substitution T G intron_variant MELA-AU 15 59187328 59187328 single base substitution C A intron_variant MELA-AU 15 59187384 59187384 single base substitution G A intron_variant MELA-AU 15 59187607 59187607 single base substitution A T intron_variant MELA-AU 15 59189919 59189919 single base substitution G A intron_variant MELA-AU 15 59190251 59190251 single base substitution G A intron_variant MELA-AU 15 59190326 59190326 single base substitution G A intron_variant MELA-AU 15 59190986 59190986 single base substitution G A intron_variant MELA-AU 15 59192073 59192073 single base substitution A C intron_variant MELA-AU 15 59192153 59192153 single base substitution G A intron_variant MELA-AU 15 59192292 59192292 single base substitution T C intron_variant MELA-AU 15 59192642 59192642 single base substitution G A intron_variant MELA-AU 15 59194516 59194516 single base substitution C T intron_variant MELA-AU 15 59194610 59194610 single base substitution G A intron_variant MELA-AU 15 59194782 59194782 single base substitution G A intron_variant MELA-AU 15 59195240 59195240 single base substitution A G intron_variant MELA-AU 15 59196589 59196589 single base substitution A G intron_variant MELA-AU 15 59196617 59196617 single base substitution G A intron_variant MELA-AU 15 59197091 59197091 single base substitution G A intron_variant MELA-AU 15 59197482 59197482 single base substitution T C intron_variant MELA-AU 15 59197849 59197849 single base substitution T A intron_variant MELA-AU 15 59197850 59197850 single base substitution A G intron_variant MELA-AU 15 59198037 59198037 single base substitution G A intron_variant MELA-AU 15 59198424 59198424 single base substitution G A intron_variant MELA-AU 15 59198491 59198491 single base substitution C T intron_variant MELA-AU 15 59198564 59198564 single base substitution G A intron_variant MELA-AU 15 59199271 59199271 single base substitution G A intron_variant MELA-AU 15 59199724 59199724 single base substitution G A intron_variant MELA-AU 15 59199796 59199796 single base substitution G A intron_variant MELA-AU 15 59201437 59201438 deletion of <=200bp CT - intron_variant MELA-AU 15 59202145 59202145 single base substitution G A intron_variant MELA-AU 15 59203207 59203207 single base substitution T A intron_variant MELA-AU 15 59203552 59203552 single base substitution G A intron_variant MELA-AU 15 59203599 59203599 single base substitution G A intron_variant MELA-AU 15 59203658 59203658 single base substitution G A intron_variant MELA-AU 15 59204022 59204022 single base substitution G A intron_variant MELA-AU 15 59204095 59204095 single base substitution A C intron_variant MELA-AU 15 59204200 59204213 deletion of <=200bp TACAGAAAGGATGG - intron_variant MELA-AU 15 59205349 59205349 single base substitution G A intron_variant MELA-AU 15 59205836 59205836 single base substitution G A intron_variant MELA-AU 15 59205893 59205893 single base substitution G A intron_variant MELA-AU 15 59206849 59206849 single base substitution G A intron_variant MELA-AU 15 59206860 59206860 single base substitution G A intron_variant MELA-AU 15 59209191 59209191 deletion of <=200bp T - intron_variant MELA-AU 15 59210044 59210044 single base substitution G A intron_variant MELA-AU 15 59210173 59210173 single base substitution G A intron_variant MELA-AU 15 59210371 59210371 single base substitution C T intron_variant MELA-AU 15 59211204 59211204 single base substitution C T intron_variant MELA-AU 15 59211302 59211303 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59211767 59211767 single base substitution G A intron_variant MELA-AU 15 59212237 59212237 deletion of <=200bp G - intron_variant MELA-AU 15 59212241 59212241 single base substitution G A intron_variant MELA-AU 15 59212827 59212830 deletion of <=200bp AATA - intron_variant MELA-AU 15 59214003 59214003 single base substitution C T intron_variant MELA-AU 15 59214356 59214356 single base substitution C T intron_variant MELA-AU 15 59214470 59214470 single base substitution G A intron_variant MELA-AU 15 59214890 59214890 single base substitution G A intron_variant MELA-AU 15 59215465 59215465 single base substitution G A intron_variant MELA-AU 15 59216165 59216165 single base substitution C A intron_variant MELA-AU 15 59216188 59216188 single base substitution A T intron_variant MELA-AU 15 59216205 59216205 single base substitution G A intron_variant MELA-AU 15 59216588 59216588 single base substitution A G intron_variant MELA-AU 15 59220665 59220665 single base substitution A C intron_variant MELA-AU 15 59221103 59221103 single base substitution C T intron_variant MELA-AU 15 59221422 59221422 single base substitution G A intron_variant MELA-AU 15 59221635 59221635 single base substitution G A intron_variant MELA-AU 15 59221674 59221674 single base substitution G A intron_variant MELA-AU 15 59222133 59222133 single base substitution A T intron_variant MELA-AU 15 59223231 59223231 single base substitution A G intron_variant MELA-AU 15 59223799 59223799 single base substitution G A intron_variant MELA-AU 15 59224545 59224562 deletion of <=200bp TCGTAACAACCTTTGCCT - intron_variant MELA-AU 15 59225948 59225948 single base substitution G A intron_variant MELA-AU 15 59226055 59226057 multiple base substitution (>=2bp and <=200bp) CAC TGT intron_variant MELA-AU 15 59226228 59226228 single base substitution G A intron_variant MELA-AU 15 59227280 59227280 single base substitution G A intron_variant MELA-AU 15 59228181 59228181 single base substitution C T intron_variant MELA-AU 15 59229603 59229603 single base substitution C T intron_variant MELA-AU 15 59229932 59229932 single base substitution C T intron_variant MELA-AU 15 59230467 59230467 single base substitution C T intron_variant MELA-AU 15 59230898 59230898 single base substitution C T intron_variant MELA-AU 15 59231031 59231031 single base substitution T A intron_variant MELA-AU 15 59231056 59231056 single base substitution T G intron_variant MELA-AU 15 59231201 59231201 single base substitution G A intron_variant MELA-AU 15 59231211 59231211 single base substitution C T intron_variant MELA-AU 15 59231389 59231389 single base substitution C T intron_variant MELA-AU 15 59231697 59231697 single base substitution G A intron_variant MELA-AU 15 59232075 59232075 single base substitution C T intron_variant MELA-AU 15 59232080 59232080 single base substitution C T intron_variant MELA-AU 15 59232114 59232114 single base substitution T C intron_variant MELA-AU 15 59232395 59232395 single base substitution G A intron_variant MELA-AU 15 59232584 59232584 single base substitution G A intron_variant MELA-AU 15 59233401 59233401 single base substitution T G intron_variant MELA-AU 15 59234314 59234314 single base substitution G A intron_variant MELA-AU 15 59234397 59234397 single base substitution G A intron_variant MELA-AU 15 59234725 59234725 single base substitution C T intron_variant MELA-AU 15 59234793 59234793 single base substitution G A intron_variant MELA-AU 15 59235615 59235615 single base substitution C T intron_variant MELA-AU 15 59235943 59235943 single base substitution G A intron_variant MELA-AU 15 59236450 59236450 single base substitution C T intron_variant MELA-AU 15 59236510 59236510 single base substitution G A intron_variant MELA-AU 15 59236596 59236596 single base substitution G A intron_variant MELA-AU 15 59236836 59236836 single base substitution G A intron_variant MELA-AU 15 59237496 59237496 single base substitution T C intron_variant MELA-AU 15 59237711 59237711 single base substitution G A intron_variant MELA-AU 15 59237745 59237745 single base substitution T C intron_variant MELA-AU 15 59237883 59237883 single base substitution G A intron_variant MELA-AU 15 59238098 59238098 single base substitution G A intron_variant MELA-AU 15 59238440 59238440 single base substitution G A intron_variant MELA-AU 15 59238446 59238446 single base substitution G A intron_variant MELA-AU 15 59238516 59238516 single base substitution G A intron_variant MELA-AU 15 59238561 59238561 single base substitution G A intron_variant MELA-AU 15 59238998 59238999 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 59239290 59239290 single base substitution G A intron_variant MELA-AU 15 59239552 59239552 single base substitution C T intron_variant MELA-AU 15 59240482 59240482 single base substitution C T intron_variant MELA-AU 15 59240980 59240980 single base substitution C T intron_variant MELA-AU 15 59241306 59241306 single base substitution C T intron_variant MELA-AU 15 59241607 59241607 single base substitution G A intron_variant MELA-AU 15 59241784 59241784 single base substitution T G intron_variant MELA-AU 15 59241819 59241819 single base substitution G A intron_variant MELA-AU 15 59241840 59241840 single base substitution G A intron_variant MELA-AU 15 59241976 59241976 single base substitution G A intron_variant MELA-AU 15 59241982 59241982 single base substitution G A intron_variant MELA-AU 15 59241985 59241985 single base substitution A C intron_variant MELA-AU 15 59242127 59242127 single base substitution G A intron_variant MELA-AU 15 59242441 59242441 single base substitution C T intron_variant MELA-AU 15 59242811 59242811 deletion of <=200bp A - intron_variant MELA-AU 15 59243195 59243195 single base substitution C T intron_variant MELA-AU 15 59243212 59243212 single base substitution C T intron_variant MELA-AU 15 59243608 59243608 single base substitution C T intron_variant MELA-AU 15 59244010 59244010 single base substitution G A intron_variant MELA-AU 15 59244097 59244097 single base substitution G A intron_variant MELA-AU 15 59244329 59244329 single base substitution C T intron_variant MELA-AU 15 59244996 59244996 single base substitution T C intron_variant MELA-AU 15 59245156 59245156 single base substitution C T intron_variant MELA-AU 15 59245559 59245559 single base substitution T A intron_variant MELA-AU 15 59245685 59245685 single base substitution C T intron_variant MELA-AU 15 59245980 59245980 single base substitution C T intron_variant MELA-AU 15 59246392 59246392 single base substitution C T intron_variant MELA-AU 15 59246395 59246395 single base substitution G A intron_variant MELA-AU 15 59246411 59246411 single base substitution G A intron_variant MELA-AU 15 59246564 59246564 single base substitution C T intron_variant MELA-AU 15 59247991 59247991 single base substitution C T intron_variant MELA-AU 15 59248918 59248918 single base substitution C T intron_variant MELA-AU 15 59249269 59249269 single base substitution C A intron_variant MELA-AU 15 59249323 59249323 single base substitution G A intron_variant MELA-AU 15 59249400 59249400 single base substitution G A intron_variant MELA-AU 15 59249756 59249756 single base substitution G A intron_variant MELA-AU 15 59249835 59249835 single base substitution A C intron_variant MELA-AU 15 59250531 59250531 single base substitution C T intron_variant MELA-AU 15 59250615 59250615 single base substitution G A intron_variant MELA-AU 15 59250820 59250820 insertion of <=200bp - T intron_variant MELA-AU 15 59250866 59250866 single base substitution G A intron_variant MELA-AU 15 59251032 59251032 single base substitution G A intron_variant MELA-AU 15 59251452 59251452 single base substitution G A intron_variant MELA-AU 15 59251575 59251575 single base substitution G A intron_variant MELA-AU 15 59251906 59251906 single base substitution C T intron_variant MELA-AU 15 59252324 59252324 single base substitution C T intron_variant MELA-AU 15 59252471 59252472 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59252844 59252844 single base substitution A G intron_variant MELA-AU 15 59252863 59252863 single base substitution C T intron_variant MELA-AU 15 59253151 59253151 single base substitution C T intron_variant MELA-AU 15 59253961 59253961 single base substitution C T intron_variant MELA-AU 15 59254174 59254174 single base substitution A C intron_variant MELA-AU 15 59254412 59254412 single base substitution A C intron_variant MELA-AU 15 59254563 59254563 single base substitution G A intron_variant MELA-AU 15 59254762 59254762 single base substitution C T intron_variant MELA-AU 15 59255201 59255201 single base substitution A G intron_variant MELA-AU 15 59255769 59255769 single base substitution G A intron_variant MELA-AU 15 59256015 59256015 single base substitution G A intron_variant MELA-AU 15 59256181 59256181 single base substitution G A intron_variant MELA-AU 15 59256415 59256415 single base substitution C T intron_variant MELA-AU 15 59256462 59256462 single base substitution C T intron_variant MELA-AU 15 59256758 59256758 single base substitution T C intron_variant MELA-AU 15 59257008 59257008 single base substitution C T intron_variant MELA-AU 15 59257262 59257262 deletion of <=200bp A - intron_variant MELA-AU 15 59258087 59258087 single base substitution G A intron_variant MELA-AU 15 59258327 59258327 single base substitution G A intron_variant MELA-AU 15 59258338 59258338 single base substitution C T intron_variant MELA-AU 15 59258712 59258712 single base substitution C T intron_variant MELA-AU 15 59258878 59258878 single base substitution C A intron_variant MELA-AU 15 59258925 59258925 single base substitution T A intron_variant MELA-AU 15 59259010 59259010 single base substitution C T intron_variant MELA-AU 15 59259360 59259360 single base substitution C T intron_variant MELA-AU 15 59259814 59259814 single base substitution C T intron_variant MELA-AU 15 59259897 59259897 single base substitution T A intron_variant MELA-AU 15 59260182 59260182 single base substitution G A intron_variant MELA-AU 15 59260297 59260297 single base substitution G A intron_variant MELA-AU 15 59260482 59260482 single base substitution C T intron_variant MELA-AU 15 59260773 59260773 single base substitution G A intron_variant MELA-AU 15 59260819 59260819 single base substitution T C intron_variant MELA-AU 15 59260836 59260836 single base substitution C T intron_variant MELA-AU 15 59260864 59260864 single base substitution G A intron_variant MELA-AU 15 59260953 59260953 single base substitution G A intron_variant MELA-AU 15 59261224 59261224 single base substitution G A intron_variant MELA-AU 15 59261234 59261234 single base substitution C T intron_variant MELA-AU 15 59261242 59261242 single base substitution C T intron_variant MELA-AU 15 59261526 59261526 single base substitution G A intron_variant MELA-AU 15 59261531 59261531 single base substitution G A intron_variant MELA-AU 15 59261594 59261594 single base substitution C T intron_variant MELA-AU 15 59261921 59261921 single base substitution C T intron_variant MELA-AU 15 59261945 59261945 single base substitution C T intron_variant MELA-AU 15 59262102 59262102 single base substitution C T intron_variant MELA-AU 15 59262471 59262471 single base substitution C T intron_variant MELA-AU 15 59262583 59262583 single base substitution T C intron_variant MELA-AU 15 59262627 59262627 single base substitution C T intron_variant MELA-AU 15 59262629 59262629 single base substitution C T intron_variant MELA-AU 15 59262648 59262648 single base substitution G A intron_variant MELA-AU 15 59262688 59262688 single base substitution C T intron_variant MELA-AU 15 59262725 59262725 single base substitution C T intron_variant MELA-AU 15 59262994 59262994 single base substitution G A intron_variant MELA-AU 15 59263173 59263173 single base substitution C T intron_variant MELA-AU 15 59263281 59263281 single base substitution G A intron_variant MELA-AU 15 59263287 59263287 single base substitution G A intron_variant MELA-AU 15 59263579 59263579 single base substitution C T intron_variant MELA-AU 15 59263658 59263658 single base substitution C T intron_variant MELA-AU 15 59263696 59263696 single base substitution C T intron_variant MELA-AU 15 59263701 59263701 single base substitution G A intron_variant MELA-AU 15 59263806 59263806 single base substitution C T intron_variant MELA-AU 15 59264124 59264124 single base substitution C T intron_variant MELA-AU 15 59264358 59264358 single base substitution G A intron_variant MELA-AU 15 59264382 59264382 single base substitution G A intron_variant MELA-AU 15 59264828 59264828 single base substitution C T intron_variant MELA-AU 15 59265015 59265015 single base substitution C T intron_variant MELA-AU 15 59265531 59265531 single base substitution G A intron_variant MELA-AU 15 59265607 59265607 single base substitution T C intron_variant MELA-AU 15 59265750 59265750 single base substitution C T intron_variant MELA-AU 15 59265788 59265788 single base substitution G A intron_variant MELA-AU 15 59265816 59265816 single base substitution C T intron_variant MELA-AU 15 59265916 59265916 single base substitution C A intron_variant MELA-AU 15 59265918 59265918 single base substitution C T intron_variant MELA-AU 15 59265983 59265983 single base substitution G C intron_variant MELA-AU 15 59265985 59265985 single base substitution A G intron_variant MELA-AU 15 59266022 59266022 single base substitution C T intron_variant MELA-AU 15 59266107 59266107 single base substitution C T intron_variant MELA-AU 15 59266193 59266193 single base substitution C T intron_variant MELA-AU 15 59266256 59266256 single base substitution C T intron_variant MELA-AU 15 59266551 59266551 single base substitution C T intron_variant MELA-AU 15 59266701 59266701 single base substitution C T intron_variant MELA-AU 15 59266708 59266708 single base substitution T C intron_variant MELA-AU 15 59266725 59266725 single base substitution G A intron_variant MELA-AU 15 59266763 59266763 single base substitution C T intron_variant MELA-AU 15 59266805 59266805 single base substitution G A intron_variant MELA-AU 15 59267100 59267100 single base substitution T G intron_variant MELA-AU 15 59267219 59267219 single base substitution C T intron_variant MELA-AU 15 59267317 59267317 single base substitution G A intron_variant MELA-AU 15 59267607 59267607 single base substitution C T intron_variant MELA-AU 15 59267711 59267711 single base substitution T A intron_variant MELA-AU 15 59267819 59267819 single base substitution G A intron_variant MELA-AU 15 59268246 59268246 single base substitution C T intron_variant MELA-AU 15 59269139 59269139 single base substitution G A intron_variant MELA-AU 15 59269338 59269338 single base substitution G A intron_variant MELA-AU 15 59269488 59269488 single base substitution G A intron_variant MELA-AU 15 59269509 59269509 single base substitution C T intron_variant MELA-AU 15 59269572 59269572 single base substitution C T intron_variant MELA-AU 15 59270544 59270544 single base substitution C T intron_variant MELA-AU 15 59270560 59270560 single base substitution C T intron_variant MELA-AU 15 59270566 59270566 single base substitution G A intron_variant MELA-AU 15 59270607 59270607 single base substitution T A intron_variant MELA-AU 15 59270854 59270854 single base substitution C T intron_variant MELA-AU 15 59270895 59270895 single base substitution C T intron_variant MELA-AU 15 59271226 59271226 single base substitution G A intron_variant MELA-AU 15 59271302 59271302 single base substitution G A intron_variant MELA-AU 15 59271394 59271394 single base substitution C T intron_variant MELA-AU 15 59271475 59271475 single base substitution G A intron_variant MELA-AU 15 59271935 59271935 single base substitution T G intron_variant MELA-AU 15 59272422 59272422 single base substitution C T intron_variant MELA-AU 15 59272434 59272434 single base substitution G A intron_variant MELA-AU 15 59272549 59272549 single base substitution G A intron_variant MELA-AU 15 59272800 59272800 single base substitution C T intron_variant MELA-AU 15 59273059 59273059 single base substitution C T intron_variant MELA-AU 15 59273696 59273696 single base substitution C T intron_variant MELA-AU 15 59273894 59273894 single base substitution C T intron_variant MELA-AU 15 59274464 59274464 single base substitution T G intron_variant MELA-AU 15 59275171 59275171 single base substitution C T intron_variant MELA-AU 15 59275171 59275171 single base substitution C T upstream_gene_variant MELA-AU 15 59275386 59275386 single base substitution C T intron_variant MELA-AU 15 59275386 59275386 single base substitution C T upstream_gene_variant MELA-AU 15 59275406 59275406 single base substitution G A intron_variant MELA-AU 15 59275406 59275406 single base substitution G A upstream_gene_variant MELA-AU 15 59275515 59275515 single base substitution C T intron_variant MELA-AU 15 59275515 59275515 single base substitution C T upstream_gene_variant MELA-AU 15 59275608 59275608 single base substitution C T intron_variant MELA-AU 15 59275608 59275608 single base substitution C T upstream_gene_variant MELA-AU 15 59276131 59276131 single base substitution C G intron_variant MELA-AU 15 59276131 59276131 single base substitution C G upstream_gene_variant MELA-AU 15 59276413 59276413 single base substitution G A intron_variant MELA-AU 15 59276413 59276413 single base substitution G A upstream_gene_variant MELA-AU 15 59276589 59276589 single base substitution G A intron_variant MELA-AU 15 59276589 59276589 single base substitution G A upstream_gene_variant MELA-AU 15 59276591 59276591 single base substitution A G intron_variant MELA-AU 15 59276591 59276591 single base substitution A G upstream_gene_variant MELA-AU 15 59276936 59276936 single base substitution G A intron_variant MELA-AU 15 59276936 59276936 single base substitution G A upstream_gene_variant MELA-AU 15 59277013 59277013 single base substitution G A intron_variant MELA-AU 15 59277013 59277013 single base substitution G A upstream_gene_variant MELA-AU 15 59277411 59277411 single base substitution A G intron_variant MELA-AU 15 59277411 59277411 single base substitution A G upstream_gene_variant MELA-AU 15 59277466 59277466 single base substitution C T intron_variant MELA-AU 15 59277466 59277466 single base substitution C T upstream_gene_variant MELA-AU 15 59277559 59277559 single base substitution C T intron_variant MELA-AU 15 59277559 59277559 single base substitution C T upstream_gene_variant MELA-AU 15 59278029 59278029 single base substitution T A intron_variant MELA-AU 15 59278029 59278029 single base substitution T A upstream_gene_variant MELA-AU 15 59278684 59278684 single base substitution G A intron_variant MELA-AU 15 59278684 59278684 single base substitution G A upstream_gene_variant MELA-AU 15 59279613 59279613 single base substitution G A intron_variant MELA-AU 15 59279613 59279613 single base substitution G A upstream_gene_variant MELA-AU 15 59279842 59279842 single base substitution G A intron_variant MELA-AU 15 59279842 59279842 single base substitution G A upstream_gene_variant MELA-AU 15 59280127 59280127 single base substitution T C 5_prime_UTR_variant MELA-AU 15 59280127 59280127 single base substitution T C intron_variant MELA-AU 15 59280127 59280127 single base substitution T C upstream_gene_variant MELA-AU 15 59281148 59281148 single base substitution A G intron_variant MELA-AU 15 59281395 59281395 single base substitution C T intron_variant MELA-AU 15 59282534 59282534 single base substitution C T intron_variant MELA-AU 15 59282607 59282607 single base substitution C T intron_variant MELA-AU 15 59283813 59283813 single base substitution T C intron_variant MELA-AU 15 59284522 59284522 single base substitution A T intron_variant MELA-AU 15 59285075 59285075 single base substitution C T intron_variant MELA-AU 15 59285603 59285604 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59287181 59287181 single base substitution C T intron_variant MELA-AU 15 59288007 59288007 single base substitution G A intron_variant MELA-AU 15 59288044 59288044 single base substitution C T intron_variant MELA-AU 15 59288150 59288150 single base substitution C T intron_variant MELA-AU 15 59288529 59288529 single base substitution C T intron_variant MELA-AU 15 59288731 59288731 single base substitution G A intron_variant MELA-AU 15 59289378 59289378 single base substitution C T intron_variant MELA-AU 15 59289387 59289387 single base substitution C T intron_variant MELA-AU 15 59290637 59290637 single base substitution C T intron_variant MELA-AU 15 59291363 59291363 single base substitution C T intron_variant MELA-AU 15 59291911 59291911 single base substitution C T intron_variant MELA-AU 15 59291984 59291984 single base substitution C T intron_variant MELA-AU 15 59292181 59292181 single base substitution C T intron_variant MELA-AU 15 59292194 59292194 single base substitution C T intron_variant MELA-AU 15 59292825 59292825 single base substitution C T intron_variant MELA-AU 15 59292881 59292881 single base substitution C T intron_variant MELA-AU 15 59293322 59293322 single base substitution C T intron_variant MELA-AU 15 59293814 59293814 single base substitution T C intron_variant MELA-AU 15 59293858 59293858 single base substitution A T intron_variant MELA-AU 15 59294580 59294580 single base substitution A G intron_variant MELA-AU 15 59294677 59294677 single base substitution A C intron_variant MELA-AU 15 59294863 59294863 single base substitution C T intron_variant MELA-AU 15 59294894 59294894 single base substitution A G intron_variant MELA-AU 15 59294967 59294967 single base substitution A T intron_variant MELA-AU 15 59294988 59294988 single base substitution C T intron_variant MELA-AU 15 59295325 59295325 single base substitution C T intron_variant MELA-AU 15 59295426 59295426 single base substitution C T intron_variant MELA-AU 15 59296249 59296249 single base substitution C T 5_prime_UTR_variant MELA-AU 15 59296249 59296249 single base substitution C T intron_variant MELA-AU 15 59298052 59298052 single base substitution A C intron_variant MELA-AU 15 59298445 59298445 single base substitution T C intron_variant MELA-AU 15 59298702 59298702 single base substitution G A intron_variant MELA-AU 15 59299084 59299084 single base substitution C T intron_variant MELA-AU 15 59299183 59299183 single base substitution C A intron_variant MELA-AU 15 59299417 59299417 single base substitution C T intron_variant MELA-AU 15 59299462 59299462 single base substitution T C intron_variant MELA-AU 15 59299472 59299472 single base substitution T C intron_variant MELA-AU 15 59300907 59300907 single base substitution C T intron_variant MELA-AU 15 59301153 59301153 single base substitution T C intron_variant MELA-AU 15 59302479 59302479 single base substitution A T intron_variant MELA-AU 15 59302609 59302609 single base substitution T A intron_variant MELA-AU 15 59302736 59302736 single base substitution G A intron_variant MELA-AU 15 59302948 59302948 single base substitution C T intron_variant MELA-AU 15 59304244 59304244 single base substitution C T intron_variant MELA-AU 15 59304260 59304260 single base substitution C A intron_variant MELA-AU 15 59305653 59305653 single base substitution C T intron_variant MELA-AU 15 59305660 59305660 single base substitution C T intron_variant MELA-AU 15 59306714 59306714 single base substitution G A intron_variant MELA-AU 15 59306814 59306814 single base substitution G C intron_variant MELA-AU 15 59307987 59307987 single base substitution G A intron_variant MELA-AU 15 59308963 59308963 single base substitution C A intron_variant MELA-AU 15 59309124 59309124 single base substitution G A intron_variant MELA-AU 15 59309388 59309388 single base substitution C T intron_variant MELA-AU 15 59309410 59309410 single base substitution T C intron_variant MELA-AU 15 59310391 59310391 single base substitution G C intron_variant MELA-AU 15 59310447 59310447 single base substitution C T intron_variant MELA-AU 15 59311233 59311233 single base substitution C T intron_variant MELA-AU 15 59312218 59312218 deletion of <=200bp G - intron_variant MELA-AU 15 59312241 59312241 single base substitution A G intron_variant MELA-AU 15 59313347 59313347 single base substitution C T intron_variant MELA-AU 15 59313418 59313418 single base substitution C T intron_variant MELA-AU 15 59313470 59313470 single base substitution C T intron_variant MELA-AU 15 59314278 59314278 single base substitution C T intron_variant MELA-AU 15 59314645 59314645 single base substitution T G intron_variant MELA-AU 15 59315235 59315235 single base substitution C T intron_variant MELA-AU 15 59315243 59315243 single base substitution C T intron_variant MELA-AU 15 59315935 59315935 single base substitution C T intron_variant MELA-AU 15 59316352 59316352 single base substitution C T intron_variant MELA-AU 15 59316510 59316510 single base substitution A T intron_variant MELA-AU 15 59316972 59316972 single base substitution C T intron_variant MELA-AU 15 59317102 59317102 single base substitution C T intron_variant MELA-AU 15 59317111 59317111 single base substitution G A intron_variant MELA-AU 15 59317572 59317572 single base substitution C T intron_variant MELA-AU 15 59318369 59318369 single base substitution G A intron_variant MELA-AU 15 59318369 59318369 single base substitution G A upstream_gene_variant MELA-AU 15 59318517 59318517 single base substitution C T intron_variant MELA-AU 15 59318517 59318517 single base substitution C T upstream_gene_variant MELA-AU 15 59318778 59318778 single base substitution T A intron_variant MELA-AU 15 59318778 59318778 single base substitution T A upstream_gene_variant MELA-AU 15 59319913 59319913 single base substitution G A intron_variant MELA-AU 15 59319913 59319913 single base substitution G A upstream_gene_variant MELA-AU 15 59320123 59320123 single base substitution C T intron_variant MELA-AU 15 59320123 59320123 single base substitution C T upstream_gene_variant MELA-AU 15 59321430 59321430 single base substitution C T intron_variant MELA-AU 15 59321430 59321430 single base substitution C T upstream_gene_variant MELA-AU 15 59322139 59322139 single base substitution C T intron_variant MELA-AU 15 59322139 59322139 single base substitution C T upstream_gene_variant MELA-AU 15 59322464 59322464 single base substitution G A intron_variant MELA-AU 15 59322464 59322464 single base substitution G A upstream_gene_variant MELA-AU 15 59322635 59322635 single base substitution C T intron_variant MELA-AU 15 59322635 59322635 single base substitution C T upstream_gene_variant MELA-AU 15 59322705 59322705 single base substitution G T intron_variant MELA-AU 15 59322705 59322705 single base substitution G T upstream_gene_variant MELA-AU 15 59323288 59323288 single base substitution C T synonymous_variant L112L 336C>T MELA-AU 15 59323288 59323288 single base substitution C T synonymous_variant L89L 267C>T MELA-AU 15 59323288 59323288 single base substitution C T upstream_gene_variant MELA-AU 15 59323460 59323460 single base substitution T C downstream_gene_variant MELA-AU 15 59323460 59323460 single base substitution T C missense_variant F147L 439T>C MELA-AU 15 59323460 59323460 single base substitution T C upstream_gene_variant MELA-AU 15 59323591 59323591 single base substitution A T downstream_gene_variant MELA-AU 15 59323591 59323591 single base substitution A T missense_variant E190D 570A>T MELA-AU 15 59323591 59323591 single base substitution A T upstream_gene_variant MELA-AU 15 59323955 59323955 single base substitution T C downstream_gene_variant MELA-AU 15 59323955 59323955 single base substitution T C intron_variant MELA-AU 15 59324056 59324056 single base substitution C T downstream_gene_variant MELA-AU 15 59324056 59324056 single base substitution C T intron_variant MELA-AU 15 59324626 59324626 single base substitution C T downstream_gene_variant MELA-AU 15 59324626 59324626 single base substitution C T intron_variant MELA-AU 15 59324746 59324746 single base substitution A T downstream_gene_variant MELA-AU 15 59324746 59324746 single base substitution A T intron_variant MELA-AU 15 59326598 59326598 single base substitution C T downstream_gene_variant MELA-AU 15 59326598 59326598 single base substitution C T intron_variant MELA-AU 15 59327491 59327491 single base substitution C T downstream_gene_variant MELA-AU 15 59327491 59327491 single base substitution C T intron_variant MELA-AU 15 59327611 59327611 single base substitution C T downstream_gene_variant MELA-AU 15 59327611 59327611 single base substitution C T intron_variant MELA-AU 15 59327652 59327652 single base substitution C T downstream_gene_variant MELA-AU 15 59327652 59327652 single base substitution C T intron_variant MELA-AU 15 59327987 59327987 single base substitution C T downstream_gene_variant MELA-AU 15 59327987 59327987 single base substitution C T intron_variant MELA-AU 15 59329929 59329929 single base substitution G A intron_variant MELA-AU 15 59330031 59330031 single base substitution C T intron_variant MELA-AU 15 59330258 59330258 single base substitution T G intron_variant MELA-AU 15 59331299 59331299 single base substitution G T intron_variant MELA-AU 15 59331521 59331521 single base substitution G A intron_variant MELA-AU 15 59331917 59331917 single base substitution C T intron_variant MELA-AU 15 59333974 59333974 single base substitution C T intron_variant MELA-AU 15 59334009 59334009 single base substitution T A intron_variant MELA-AU 15 59334219 59334219 single base substitution C T intron_variant MELA-AU 15 59334299 59334299 single base substitution C T intron_variant MELA-AU 15 59334749 59334750 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 59334789 59334789 single base substitution C T intron_variant MELA-AU 15 59334967 59334967 single base substitution C T intron_variant MELA-AU 15 59335166 59335166 single base substitution A T intron_variant MELA-AU 15 59335808 59335808 single base substitution C T intron_variant MELA-AU 15 59336263 59336263 single base substitution T G intron_variant MELA-AU 15 59337265 59337265 single base substitution C T intron_variant MELA-AU 15 59337375 59337375 single base substitution T A intron_variant MELA-AU 15 59338277 59338277 single base substitution C T intron_variant MELA-AU 15 59339415 59339415 single base substitution C T intron_variant MELA-AU 15 59339971 59339971 single base substitution C T intron_variant MELA-AU 15 59340000 59340000 single base substitution C T intron_variant MELA-AU 15 59340031 59340031 single base substitution C T intron_variant MELA-AU 15 59340688 59340688 single base substitution C A intron_variant MELA-AU 15 59340787 59340787 single base substitution A G intron_variant MELA-AU 15 59341182 59341182 single base substitution C T intron_variant MELA-AU 15 59341291 59341291 single base substitution C A intron_variant MELA-AU 15 59341405 59341405 single base substitution T C intron_variant MELA-AU 15 59341828 59341828 single base substitution C T intron_variant MELA-AU 15 59342159 59342159 single base substitution C T intron_variant MELA-AU 15 59342615 59342615 single base substitution C T intron_variant MELA-AU 15 59343066 59343066 single base substitution C T intron_variant MELA-AU 15 59343372 59343372 single base substitution G A intron_variant MELA-AU 15 59343969 59343969 single base substitution T C intron_variant MELA-AU 15 59343971 59343971 insertion of <=200bp - AATA intron_variant MELA-AU 15 59344049 59344049 single base substitution A T intron_variant MELA-AU 15 59345073 59345073 single base substitution C T intron_variant MELA-AU 15 59345085 59345085 single base substitution A G intron_variant MELA-AU 15 59345720 59345720 single base substitution C T intron_variant MELA-AU 15 59346219 59346219 single base substitution C T intron_variant MELA-AU 15 59346244 59346244 single base substitution C T intron_variant MELA-AU 15 59346509 59346509 single base substitution C T intron_variant MELA-AU 15 59346627 59346627 single base substitution C T intron_variant MELA-AU 15 59347324 59347324 single base substitution C T intron_variant MELA-AU 15 59349040 59349040 single base substitution G A intron_variant MELA-AU 15 59351081 59351081 single base substitution C T downstream_gene_variant MELA-AU 15 59351081 59351081 single base substitution C T intron_variant MELA-AU 15 59351359 59351359 single base substitution C T downstream_gene_variant MELA-AU 15 59351359 59351359 single base substitution C T intron_variant MELA-AU 15 59351701 59351701 single base substitution C T downstream_gene_variant MELA-AU 15 59351701 59351701 single base substitution C T intron_variant MELA-AU 15 59351764 59351764 single base substitution C T downstream_gene_variant MELA-AU 15 59351764 59351764 single base substitution C T intron_variant MELA-AU 15 59351772 59351772 single base substitution G T downstream_gene_variant MELA-AU 15 59351772 59351772 single base substitution G T intron_variant MELA-AU 15 59351956 59351956 single base substitution T C downstream_gene_variant MELA-AU 15 59351956 59351956 single base substitution T C intron_variant MELA-AU 15 59352784 59352784 single base substitution C T downstream_gene_variant MELA-AU 15 59352784 59352784 single base substitution C T intron_variant MELA-AU 15 59353604 59353604 single base substitution C T downstream_gene_variant MELA-AU 15 59353604 59353604 single base substitution C T intron_variant MELA-AU 15 59353651 59353651 single base substitution C T downstream_gene_variant MELA-AU 15 59353651 59353651 single base substitution C T intron_variant MELA-AU 15 59354363 59354363 single base substitution C T downstream_gene_variant MELA-AU 15 59354363 59354363 single base substitution C T intron_variant MELA-AU 15 59355493 59355493 single base substitution C T downstream_gene_variant MELA-AU 15 59355493 59355493 single base substitution C T intron_variant MELA-AU 15 59355581 59355581 single base substitution C T downstream_gene_variant MELA-AU 15 59355581 59355581 single base substitution C T intron_variant MELA-AU 15 59355677 59355677 single base substitution C T downstream_gene_variant MELA-AU 15 59355677 59355677 single base substitution C T intron_variant MELA-AU 15 59355734 59355734 single base substitution A G downstream_gene_variant MELA-AU 15 59355734 59355734 single base substitution A G intron_variant MELA-AU 15 59355819 59355819 single base substitution C G downstream_gene_variant MELA-AU 15 59355819 59355819 single base substitution C G intron_variant MELA-AU 15 59355888 59355888 single base substitution G A intron_variant MELA-AU 15 59355902 59355902 single base substitution C T intron_variant MELA-AU 15 59356917 59356917 single base substitution G A intron_variant MELA-AU 15 59357070 59357070 single base substitution G A intron_variant MELA-AU 15 59358844 59358844 single base substitution C T intron_variant MELA-AU 15 59359153 59359153 single base substitution C T synonymous_variant H519H 1557C>T MELA-AU 15 59359471 59359471 single base substitution C T intron_variant MELA-AU 15 59359504 59359505 multiple base substitution (>=2bp and <=200bp) TC AT intron_variant MELA-AU 15 59359561 59359561 single base substitution C T intron_variant MELA-AU 15 59359986 59359987 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 59361387 59361387 single base substitution C T intron_variant MELA-AU 15 59361582 59361582 single base substitution A C intron_variant MELA-AU 15 59362530 59362530 single base substitution C T intron_variant MELA-AU 15 59362733 59362733 single base substitution A G intron_variant MELA-AU 15 59362921 59362921 insertion of <=200bp - T intron_variant MELA-AU 15 59362925 59362925 single base substitution C G intron_variant MELA-AU 15 59363254 59363254 single base substitution T C intron_variant MELA-AU 15 59363666 59363666 single base substitution G T intron_variant MELA-AU 15 59363998 59363998 single base substitution C T intron_variant MELA-AU 15 59364645 59364645 single base substitution C T intron_variant MELA-AU 15 59364886 59364886 single base substitution C T intron_variant MELA-AU 15 59365304 59365304 single base substitution G A intron_variant MELA-AU 15 59365696 59365696 single base substitution A T intron_variant MELA-AU 15 59366002 59366002 single base substitution A C intron_variant MELA-AU 15 59366214 59366214 single base substitution G A intron_variant MELA-AU 15 59366260 59366260 single base substitution A G intron_variant MELA-AU 15 59367718 59367718 single base substitution C T intron_variant MELA-AU 15 59367912 59367912 single base substitution T A intron_variant MELA-AU 15 59368253 59368253 single base substitution C T missense_variant S596F 1787C>T MELA-AU 15 59368253 59368253 single base substitution C T upstream_gene_variant MELA-AU 15 59368313 59368313 single base substitution C T missense_variant S616L 1847C>T MELA-AU 15 59368313 59368313 single base substitution C T upstream_gene_variant MELA-AU 15 59368943 59368943 single base substitution C T intron_variant MELA-AU 15 59368943 59368943 single base substitution C T upstream_gene_variant MELA-AU 15 59369570 59369570 single base substitution C A intron_variant MELA-AU 15 59369570 59369570 single base substitution C A upstream_gene_variant MELA-AU 15 59370667 59370667 single base substitution G T intron_variant MELA-AU 15 59370667 59370667 single base substitution G T upstream_gene_variant MELA-AU 15 59371272 59371272 single base substitution G A intron_variant MELA-AU 15 59371272 59371272 single base substitution G A upstream_gene_variant MELA-AU 15 59372410 59372410 single base substitution C T intron_variant MELA-AU 15 59372410 59372410 single base substitution C T upstream_gene_variant MELA-AU 15 59372661 59372661 single base substitution C T intron_variant MELA-AU 15 59372661 59372661 single base substitution C T upstream_gene_variant MELA-AU 15 59373529 59373529 single base substitution C T intron_variant MELA-AU 15 59373529 59373529 single base substitution C T upstream_gene_variant MELA-AU 15 59374005 59374005 single base substitution C T intron_variant MELA-AU 15 59374005 59374005 single base substitution C T upstream_gene_variant MELA-AU 15 59374822 59374822 single base substitution C T intron_variant MELA-AU 15 59374822 59374822 single base substitution C T upstream_gene_variant MELA-AU 15 59374921 59374921 single base substitution C T intron_variant MELA-AU 15 59374921 59374921 single base substitution C T upstream_gene_variant MELA-AU 15 59375649 59375649 single base substitution A T intron_variant MELA-AU 15 59375649 59375649 single base substitution A T upstream_gene_variant MELA-AU 15 59375703 59375703 single base substitution C G intron_variant MELA-AU 15 59375703 59375703 single base substitution C G upstream_gene_variant MELA-AU 15 59375734 59375734 single base substitution C T intron_variant MELA-AU 15 59375734 59375734 single base substitution C T upstream_gene_variant MELA-AU 15 59376980 59376980 single base substitution C T downstream_gene_variant MELA-AU 15 59376980 59376980 single base substitution C T intron_variant MELA-AU 15 59376980 59376980 single base substitution C T upstream_gene_variant MELA-AU 15 59377149 59377149 single base substitution C T downstream_gene_variant MELA-AU 15 59377149 59377149 single base substitution C T intron_variant MELA-AU 15 59377149 59377149 single base substitution C T upstream_gene_variant MELA-AU 15 59377309 59377309 single base substitution C T downstream_gene_variant MELA-AU 15 59377309 59377309 single base substitution C T intron_variant MELA-AU 15 59377309 59377309 single base substitution C T upstream_gene_variant MELA-AU 15 59377590 59377590 single base substitution C T downstream_gene_variant MELA-AU 15 59377590 59377590 single base substitution C T intron_variant MELA-AU 15 59377590 59377590 single base substitution C T upstream_gene_variant MELA-AU 15 59377627 59377627 single base substitution C A downstream_gene_variant MELA-AU 15 59377627 59377627 single base substitution C A intron_variant MELA-AU 15 59377627 59377627 single base substitution C A upstream_gene_variant MELA-AU 15 59378028 59378028 single base substitution C T downstream_gene_variant MELA-AU 15 59378028 59378028 single base substitution C T intron_variant MELA-AU 15 59379244 59379244 single base substitution G A downstream_gene_variant MELA-AU 15 59379244 59379244 single base substitution G A intron_variant MELA-AU 15 59379391 59379391 single base substitution C T downstream_gene_variant MELA-AU 15 59379391 59379391 single base substitution C T intron_variant MELA-AU 15 59379641 59379641 single base substitution C T downstream_gene_variant MELA-AU 15 59379641 59379641 single base substitution C T intron_variant MELA-AU 15 59380942 59380942 single base substitution T A downstream_gene_variant MELA-AU 15 59380942 59380942 single base substitution T A intron_variant MELA-AU 15 59380942 59380942 single base substitution T A upstream_gene_variant MELA-AU 15 59382092 59382092 single base substitution C T downstream_gene_variant MELA-AU 15 59382092 59382092 single base substitution C T intron_variant MELA-AU 15 59382092 59382092 single base substitution C T upstream_gene_variant MELA-AU 15 59382731 59382731 single base substitution C T downstream_gene_variant MELA-AU 15 59382731 59382731 single base substitution C T intron_variant MELA-AU 15 59382731 59382731 single base substitution C T upstream_gene_variant MELA-AU 15 59383098 59383098 insertion of <=200bp - TATA downstream_gene_variant MELA-AU 15 59383098 59383098 insertion of <=200bp - TATA intron_variant MELA-AU 15 59383098 59383098 insertion of <=200bp - TATA upstream_gene_variant MELA-AU 15 59383227 59383227 single base substitution T C downstream_gene_variant MELA-AU 15 59383227 59383227 single base substitution T C intron_variant MELA-AU 15 59383227 59383227 single base substitution T C upstream_gene_variant MELA-AU 15 59383543 59383543 single base substitution C T downstream_gene_variant MELA-AU 15 59383543 59383543 single base substitution C T intron_variant MELA-AU 15 59383543 59383543 single base substitution C T upstream_gene_variant MELA-AU 15 59384227 59384227 single base substitution T A downstream_gene_variant MELA-AU 15 59384227 59384227 single base substitution T A intron_variant MELA-AU 15 59384227 59384227 single base substitution T A upstream_gene_variant MELA-AU 15 59384974 59384974 single base substitution C T downstream_gene_variant MELA-AU 15 59384974 59384974 single base substitution C T intron_variant MELA-AU 15 59384974 59384974 single base substitution C T upstream_gene_variant MELA-AU 15 59385183 59385183 single base substitution A G downstream_gene_variant MELA-AU 15 59385183 59385183 single base substitution A G intron_variant MELA-AU 15 59385183 59385183 single base substitution A G upstream_gene_variant MELA-AU 15 59385399 59385399 single base substitution C T downstream_gene_variant MELA-AU 15 59385399 59385399 single base substitution C T intron_variant MELA-AU 15 59385399 59385399 single base substitution C T upstream_gene_variant MELA-AU 15 59386313 59386313 single base substitution T A downstream_gene_variant MELA-AU 15 59386313 59386313 single base substitution T A intron_variant MELA-AU 15 59386895 59386895 single base substitution T A downstream_gene_variant MELA-AU 15 59386895 59386895 single base substitution T A intron_variant MELA-AU 15 59387141 59387141 single base substitution C T 3_prime_UTR_variant MELA-AU 15 59387141 59387141 single base substitution C T downstream_gene_variant MELA-AU 15 59387141 59387141 single base substitution C T exon_variant MELA-AU 15 59387365 59387381 deletion of <=200bp TTGCACATATTATGGGC - 3_prime_UTR_variant MELA-AU 15 59387365 59387381 deletion of <=200bp TTGCACATATTATGGGC - downstream_gene_variant MELA-AU 15 59387365 59387381 deletion of <=200bp TTGCACATATTATGGGC - exon_variant MELA-AU 15 59387581 59387581 single base substitution C T 3_prime_UTR_variant MELA-AU 15 59387581 59387581 single base substitution C T downstream_gene_variant MELA-AU 15 59387581 59387581 single base substitution C T exon_variant MELA-AU 15 59388836 59388836 single base substitution G A 3_prime_UTR_variant MELA-AU 15 59388836 59388836 single base substitution G A downstream_gene_variant MELA-AU 15 59388978 59388978 single base substitution C A 3_prime_UTR_variant MELA-AU 15 59388978 59388978 single base substitution C A downstream_gene_variant MELA-AU 15 59389606 59389606 single base substitution C T 3_prime_UTR_variant MELA-AU 15 59389606 59389606 single base substitution C T downstream_gene_variant MELA-AU 15 59390088 59390088 single base substitution C T downstream_gene_variant MELA-AU 15 59391051 59391051 single base substitution G A downstream_gene_variant MELA-AU 15 59391108 59391108 single base substitution C T downstream_gene_variant MELA-AU 15 59391400 59391400 single base substitution T A downstream_gene_variant MELA-AU 15 59391419 59391419 single base substitution C T downstream_gene_variant MELA-AU 15 59392037 59392037 single base substitution A G downstream_gene_variant MELA-AU 15 59393360 59393360 single base substitution C T downstream_gene_variant MELA-AU 15 59393550 59393550 single base substitution G A downstream_gene_variant MELA-AU 15 59393909 59393909 single base substitution G A downstream_gene_variant ORCA-IN 15 59175842 59175842 single base substitution C A intron_variant ORCA-IN 15 59177550 59177550 single base substitution G C intron_variant ORCA-IN 15 59227428 59227428 single base substitution C G intron_variant ORCA-IN 15 59234864 59234864 single base substitution G A intron_variant ORCA-IN 15 59242874 59242874 single base substitution G C intron_variant ORCA-IN 15 59251023 59251023 single base substitution C T intron_variant ORCA-IN 15 59279343 59279343 single base substitution G C intron_variant ORCA-IN 15 59279343 59279343 single base substitution G C upstream_gene_variant ORCA-IN 15 59290326 59290326 single base substitution T A intron_variant ORCA-IN 15 59291911 59291911 single base substitution C T intron_variant ORCA-IN 15 59353371 59353371 single base substitution T C downstream_gene_variant ORCA-IN 15 59353371 59353371 single base substitution T C intron_variant ORCA-IN 15 59376343 59376343 deletion of <=200bp C - exon_variant ORCA-IN 15 59376343 59376343 deletion of <=200bp C - frameshift_variant R771 ORCA-IN 15 59376343 59376343 deletion of <=200bp C - frameshift_variant R780 ORCA-IN 15 59376343 59376343 deletion of <=200bp C - upstream_gene_variant OV-AU 15 59157181 59157181 single base substitution A T upstream_gene_variant OV-AU 15 59160710 59160710 single base substitution A C intron_variant OV-AU 15 59161463 59161463 single base substitution T C intron_variant OV-AU 15 59171699 59171699 single base substitution G T intron_variant OV-AU 15 59217020 59217020 single base substitution T C intron_variant OV-AU 15 59217830 59217830 single base substitution C T intron_variant OV-AU 15 59218929 59218929 single base substitution T G intron_variant OV-AU 15 59223170 59223170 single base substitution C A intron_variant OV-AU 15 59228447 59228447 single base substitution C G intron_variant OV-AU 15 59229771 59229771 single base substitution G A intron_variant OV-AU 15 59233508 59233508 single base substitution T A intron_variant OV-AU 15 59241476 59241476 single base substitution T C intron_variant OV-AU 15 59241981 59241981 single base substitution C T intron_variant OV-AU 15 59244033 59244033 single base substitution C G intron_variant OV-AU 15 59254606 59254606 single base substitution C G intron_variant OV-AU 15 59257467 59257467 single base substitution A G intron_variant OV-AU 15 59258369 59258369 single base substitution G C intron_variant OV-AU 15 59259158 59259158 single base substitution C A intron_variant OV-AU 15 59260027 59260027 single base substitution C T intron_variant OV-AU 15 59265577 59265577 single base substitution T G intron_variant OV-AU 15 59266762 59266762 single base substitution C T intron_variant OV-AU 15 59276976 59276976 single base substitution C T intron_variant OV-AU 15 59276976 59276976 single base substitution C T upstream_gene_variant OV-AU 15 59278125 59278125 single base substitution C A intron_variant OV-AU 15 59278125 59278125 single base substitution C A upstream_gene_variant OV-AU 15 59280689 59280689 single base substitution G T intron_variant OV-AU 15 59291716 59291716 single base substitution G A intron_variant OV-AU 15 59292620 59292620 single base substitution G A intron_variant OV-AU 15 59301008 59301008 single base substitution T G intron_variant OV-AU 15 59301283 59301283 single base substitution C T intron_variant OV-AU 15 59304747 59304747 single base substitution G A intron_variant OV-AU 15 59314183 59314183 single base substitution C T intron_variant OV-AU 15 59315172 59315172 single base substitution G A intron_variant OV-AU 15 59344006 59344006 single base substitution G A intron_variant OV-AU 15 59344280 59344280 single base substitution G C intron_variant OV-AU 15 59347028 59347028 single base substitution A G intron_variant OV-AU 15 59353725 59353725 single base substitution T A downstream_gene_variant OV-AU 15 59353725 59353725 single base substitution T A intron_variant OV-AU 15 59355809 59355809 single base substitution G T downstream_gene_variant OV-AU 15 59355809 59355809 single base substitution G T intron_variant OV-AU 15 59361018 59361018 single base substitution G T intron_variant OV-AU 15 59379657 59379657 single base substitution C T downstream_gene_variant OV-AU 15 59379657 59379657 single base substitution C T intron_variant OV-US 15 59384740 59384740 single base substitution A T downstream_gene_variant OV-US 15 59384740 59384740 single base substitution A T exon_variant OV-US 15 59384740 59384740 single base substitution A T missense_variant K915I 2744A>T OV-US 15 59384740 59384740 single base substitution A T missense_variant K923I 2768A>T OV-US 15 59384740 59384740 single base substitution A T missense_variant K924I 2771A>T OV-US 15 59384740 59384740 single base substitution A T missense_variant K932I 2795A>T OV-US 15 59384740 59384740 single base substitution A T upstream_gene_variant PACA-AU 15 59152563 59152563 single base substitution A G upstream_gene_variant PACA-AU 15 59153657 59153657 single base substitution A G upstream_gene_variant PACA-AU 15 59156231 59156231 single base substitution C T upstream_gene_variant PACA-AU 15 59173516 59173516 single base substitution G A intron_variant PACA-AU 15 59175074 59175074 single base substitution G A intron_variant PACA-AU 15 59178468 59178468 single base substitution T G intron_variant PACA-AU 15 59193827 59193873 deletion of <=200bp ACGTCACTCAGTTCACAGGTACTCTTAGCTAAGATATACTATTCAAA - intron_variant PACA-AU 15 59193880 59193880 single base substitution C G intron_variant PACA-AU 15 59194052 59194052 single base substitution C A intron_variant PACA-AU 15 59206538 59206538 single base substitution A C intron_variant PACA-AU 15 59208021 59208021 single base substitution G A intron_variant PACA-AU 15 59214399 59214399 single base substitution A C intron_variant PACA-AU 15 59221980 59221980 single base substitution C T intron_variant PACA-AU 15 59222684 59222684 single base substitution T C intron_variant PACA-AU 15 59223540 59223540 single base substitution T C intron_variant PACA-AU 15 59225776 59225776 single base substitution A C intron_variant PACA-AU 15 59227536 59227536 single base substitution C T intron_variant PACA-AU 15 59231280 59231280 single base substitution T G intron_variant PACA-AU 15 59231397 59231397 single base substitution T G intron_variant PACA-AU 15 59243911 59243911 single base substitution G T intron_variant PACA-AU 15 59257454 59257454 single base substitution A G intron_variant PACA-AU 15 59259202 59259202 single base substitution C T intron_variant PACA-AU 15 59275308 59275310 deletion of <=200bp TAG - intron_variant PACA-AU 15 59275308 59275310 deletion of <=200bp TAG - upstream_gene_variant PACA-AU 15 59275649 59275649 single base substitution C A intron_variant PACA-AU 15 59275649 59275649 single base substitution C A upstream_gene_variant PACA-AU 15 59284759 59284759 single base substitution G A intron_variant PACA-AU 15 59284855 59284855 deletion of <=200bp A - intron_variant PACA-AU 15 59306108 59306108 single base substitution G A intron_variant PACA-AU 15 59316799 59316799 single base substitution C T intron_variant PACA-AU 15 59319517 59319517 single base substitution G T intron_variant PACA-AU 15 59319517 59319517 single base substitution G T upstream_gene_variant PACA-AU 15 59326614 59326614 single base substitution A T downstream_gene_variant PACA-AU 15 59326614 59326614 single base substitution A T intron_variant PACA-AU 15 59342690 59342691 deletion of <=200bp AG - intron_variant PACA-AU 15 59343549 59343549 single base substitution C T intron_variant PACA-AU 15 59343984 59343984 single base substitution A T intron_variant PACA-AU 15 59347621 59347621 single base substitution A G intron_variant PACA-AU 15 59359208 59359208 single base substitution C G missense_variant P538A 1612C>G PACA-AU 15 59360423 59360425 deletion of <=200bp AAC - intron_variant PACA-AU 15 59366575 59366575 single base substitution T C intron_variant PACA-AU 15 59377525 59377525 single base substitution A G downstream_gene_variant PACA-AU 15 59377525 59377525 single base substitution A G intron_variant PACA-AU 15 59377525 59377525 single base substitution A G upstream_gene_variant PACA-AU 15 59381896 59381896 single base substitution C T downstream_gene_variant PACA-AU 15 59381896 59381896 single base substitution C T exon_variant PACA-AU 15 59381896 59381896 single base substitution C T missense_variant R861C 2581C>T PACA-AU 15 59381896 59381896 single base substitution C T missense_variant R870C 2608C>T PACA-AU 15 59381896 59381896 single base substitution C T upstream_gene_variant PACA-AU 15 59384851 59384851 single base substitution T A downstream_gene_variant PACA-AU 15 59384851 59384851 single base substitution T A intron_variant PACA-AU 15 59384851 59384851 single base substitution T A upstream_gene_variant PACA-AU 15 59385750 59385750 single base substitution C A downstream_gene_variant PACA-AU 15 59385750 59385750 single base substitution C A intron_variant PACA-AU 15 59386493 59386493 deletion of <=200bp T - downstream_gene_variant PACA-AU 15 59386493 59386493 deletion of <=200bp T - intron_variant PACA-AU 15 59391174 59391174 single base substitution C T downstream_gene_variant PACA-CA 15 59154902 59154902 insertion of <=200bp - A upstream_gene_variant PACA-CA 15 59155177 59155177 single base substitution A T upstream_gene_variant PACA-CA 15 59158593 59158593 single base substitution C A intron_variant PACA-CA 15 59158594 59158594 single base substitution T C intron_variant PACA-CA 15 59160840 59160840 single base substitution G T intron_variant PACA-CA 15 59163847 59163848 deletion of <=200bp TT - intron_variant PACA-CA 15 59164459 59164459 single base substitution A T intron_variant PACA-CA 15 59164703 59164703 single base substitution A T intron_variant PACA-CA 15 59170296 59170296 single base substitution A T intron_variant PACA-CA 15 59178346 59178346 single base substitution C T intron_variant PACA-CA 15 59178583 59178583 single base substitution A G intron_variant PACA-CA 15 59179690 59179690 single base substitution C T intron_variant PACA-CA 15 59179785 59179785 single base substitution G A intron_variant PACA-CA 15 59180375 59180375 single base substitution G C intron_variant PACA-CA 15 59182635 59182635 insertion of <=200bp - CT intron_variant PACA-CA 15 59183459 59183459 single base substitution A T intron_variant PACA-CA 15 59183639 59183639 single base substitution G A intron_variant PACA-CA 15 59186626 59186626 single base substitution G T intron_variant PACA-CA 15 59190987 59190987 deletion of <=200bp A - intron_variant PACA-CA 15 59193006 59193006 single base substitution C T intron_variant PACA-CA 15 59193542 59193542 insertion of <=200bp - T intron_variant PACA-CA 15 59202335 59202335 single base substitution G A intron_variant PACA-CA 15 59205724 59205724 single base substitution T C intron_variant PACA-CA 15 59205877 59205877 single base substitution G C intron_variant PACA-CA 15 59206258 59206258 single base substitution C T intron_variant PACA-CA 15 59206735 59206735 single base substitution G T intron_variant PACA-CA 15 59207061 59207061 single base substitution T C intron_variant PACA-CA 15 59209412 59209413 deletion of <=200bp CT - intron_variant PACA-CA 15 59211424 59211424 insertion of <=200bp - T intron_variant PACA-CA 15 59212880 59212880 single base substitution C T intron_variant PACA-CA 15 59213881 59213881 single base substitution G C intron_variant PACA-CA 15 59216528 59216528 single base substitution G A intron_variant PACA-CA 15 59218187 59218187 single base substitution A G intron_variant PACA-CA 15 59218224 59218224 single base substitution T C intron_variant PACA-CA 15 59219343 59219343 deletion of <=200bp A - intron_variant PACA-CA 15 59221011 59221011 single base substitution G A intron_variant PACA-CA 15 59228688 59228688 single base substitution C A intron_variant PACA-CA 15 59228976 59228976 deletion of <=200bp T - intron_variant PACA-CA 15 59232548 59232548 single base substitution C T intron_variant PACA-CA 15 59233234 59233234 single base substitution A G intron_variant PACA-CA 15 59239127 59239127 single base substitution G A intron_variant PACA-CA 15 59239583 59239583 single base substitution A G intron_variant PACA-CA 15 59243704 59243704 single base substitution A T intron_variant PACA-CA 15 59248032 59248032 insertion of <=200bp - ATAC intron_variant PACA-CA 15 59251491 59251491 single base substitution G C intron_variant PACA-CA 15 59254944 59254944 insertion of <=200bp - T intron_variant PACA-CA 15 59255111 59255111 single base substitution T G intron_variant PACA-CA 15 59255112 59255112 single base substitution C T intron_variant PACA-CA 15 59257531 59257531 single base substitution A G intron_variant PACA-CA 15 59262111 59262111 single base substitution A T intron_variant PACA-CA 15 59262391 59262391 insertion of <=200bp - T intron_variant PACA-CA 15 59262690 59262690 deletion of <=200bp T - intron_variant PACA-CA 15 59277614 59277614 single base substitution G A intron_variant PACA-CA 15 59277614 59277614 single base substitution G A upstream_gene_variant PACA-CA 15 59286509 59286509 single base substitution A T intron_variant PACA-CA 15 59287929 59287929 single base substitution C A intron_variant PACA-CA 15 59288935 59288935 single base substitution A G intron_variant PACA-CA 15 59290013 59290013 single base substitution C A intron_variant PACA-CA 15 59296909 59296924 deletion of <=200bp TAAAGTTGCCCAAATA - intron_variant PACA-CA 15 59297529 59297529 single base substitution G C intron_variant PACA-CA 15 59300416 59300416 single base substitution T G intron_variant PACA-CA 15 59305455 59305455 single base substitution C T intron_variant PACA-CA 15 59307713 59307713 single base substitution C G intron_variant PACA-CA 15 59308263 59308263 single base substitution C A intron_variant PACA-CA 15 59312565 59312565 single base substitution T A intron_variant PACA-CA 15 59314792 59314792 single base substitution A G intron_variant PACA-CA 15 59315985 59315985 deletion of <=200bp T - intron_variant PACA-CA 15 59317015 59317020 deletion of <=200bp AACACT - intron_variant PACA-CA 15 59317586 59317586 single base substitution T C intron_variant PACA-CA 15 59321437 59321437 single base substitution G A intron_variant PACA-CA 15 59321437 59321437 single base substitution G A upstream_gene_variant PACA-CA 15 59325104 59325104 single base substitution T A downstream_gene_variant PACA-CA 15 59325104 59325104 single base substitution T A intron_variant PACA-CA 15 59326718 59326718 single base substitution G C downstream_gene_variant PACA-CA 15 59326718 59326718 single base substitution G C intron_variant PACA-CA 15 59327626 59327626 single base substitution C G downstream_gene_variant PACA-CA 15 59327626 59327626 single base substitution C G intron_variant PACA-CA 15 59328422 59328422 single base substitution A C intron_variant PACA-CA 15 59330756 59330756 single base substitution G A intron_variant PACA-CA 15 59335810 59335810 single base substitution G A intron_variant PACA-CA 15 59339248 59339248 single base substitution C A intron_variant PACA-CA 15 59339338 59339338 single base substitution C T intron_variant PACA-CA 15 59339680 59339680 single base substitution C G intron_variant PACA-CA 15 59341299 59341299 single base substitution T C intron_variant PACA-CA 15 59342700 59342700 single base substitution T C intron_variant PACA-CA 15 59348174 59348174 single base substitution T A intron_variant PACA-CA 15 59350638 59350638 single base substitution T C missense_variant S152P 454T>C PACA-CA 15 59350638 59350638 single base substitution T C missense_variant S419P 1255T>C PACA-CA 15 59350709 59350709 single base substitution T C synonymous_variant A175A 525T>C PACA-CA 15 59350709 59350709 single base substitution T C synonymous_variant A442A 1326T>C PACA-CA 15 59350823 59350823 single base substitution C T 3_prime_UTR_variant PACA-CA 15 59350823 59350823 single base substitution C T intron_variant PACA-CA 15 59353003 59353003 insertion of <=200bp - TTT downstream_gene_variant PACA-CA 15 59353003 59353003 insertion of <=200bp - TTT intron_variant PACA-CA 15 59358046 59358046 insertion of <=200bp - A intron_variant PACA-CA 15 59358446 59358446 single base substitution G C intron_variant PACA-CA 15 59358808 59358808 single base substitution C G intron_variant PACA-CA 15 59359517 59359517 single base substitution C T intron_variant PACA-CA 15 59360823 59360823 single base substitution T A intron_variant PACA-CA 15 59364048 59364048 single base substitution A C intron_variant PACA-CA 15 59367068 59367068 single base substitution G A intron_variant PACA-CA 15 59368279 59368279 single base substitution C T stop_gained Q605* 1813C>T PACA-CA 15 59368279 59368279 single base substitution C T upstream_gene_variant PACA-CA 15 59368686 59368686 single base substitution T C intron_variant PACA-CA 15 59368686 59368686 single base substitution T C upstream_gene_variant PACA-CA 15 59368883 59368883 single base substitution A G intron_variant PACA-CA 15 59368883 59368883 single base substitution A G upstream_gene_variant PACA-CA 15 59369391 59369391 single base substitution A G intron_variant PACA-CA 15 59369391 59369391 single base substitution A G upstream_gene_variant PACA-CA 15 59369402 59369402 single base substitution T C intron_variant PACA-CA 15 59369402 59369402 single base substitution T C upstream_gene_variant PACA-CA 15 59369730 59369730 single base substitution A G intron_variant PACA-CA 15 59369730 59369730 single base substitution A G upstream_gene_variant PACA-CA 15 59370113 59370113 single base substitution T C intron_variant PACA-CA 15 59370113 59370113 single base substitution T C upstream_gene_variant PACA-CA 15 59376937 59376937 single base substitution C G downstream_gene_variant PACA-CA 15 59376937 59376937 single base substitution C G intron_variant PACA-CA 15 59376937 59376937 single base substitution C G upstream_gene_variant PACA-CA 15 59386267 59386267 single base substitution C T downstream_gene_variant PACA-CA 15 59386267 59386267 single base substitution C T intron_variant PACA-CA 15 59387166 59387166 single base substitution G C 3_prime_UTR_variant PACA-CA 15 59387166 59387166 single base substitution G C downstream_gene_variant PACA-CA 15 59387166 59387166 single base substitution G C exon_variant PACA-CA 15 59388412 59388412 single base substitution A G 3_prime_UTR_variant PACA-CA 15 59388412 59388412 single base substitution A G downstream_gene_variant PACA-CA 15 59388412 59388412 single base substitution A G exon_variant PACA-CA 15 59392478 59392478 single base substitution T C downstream_gene_variant PAEN-AU 15 59226050 59226050 single base substitution T G intron_variant PAEN-AU 15 59226580 59226580 single base substitution T G intron_variant PAEN-AU 15 59239930 59239930 single base substitution C A intron_variant PAEN-AU 15 59258022 59258022 single base substitution T G intron_variant PAEN-AU 15 59288711 59288711 single base substitution T G intron_variant PAEN-AU 15 59363319 59363319 single base substitution A G intron_variant PAEN-IT 15 59178913 59178913 single base substitution A G intron_variant PAEN-IT 15 59273287 59273287 single base substitution C T intron_variant PAEN-IT 15 59274460 59274460 single base substitution C G intron_variant PAEN-IT 15 59304702 59304702 single base substitution A T intron_variant PAEN-IT 15 59316252 59316252 single base substitution C T intron_variant PAEN-IT 15 59328078 59328078 single base substitution T A downstream_gene_variant PAEN-IT 15 59328078 59328078 single base substitution T A intron_variant PAEN-IT 15 59350569 59350569 single base substitution C A missense_variant P129T 385C>A PAEN-IT 15 59350569 59350569 single base substitution C A missense_variant P396T 1186C>A PBCA-DE 15 59160150 59160150 single base substitution G A intron_variant PBCA-DE 15 59163110 59163110 insertion of <=200bp - A intron_variant PBCA-DE 15 59163633 59163633 single base substitution C G intron_variant PBCA-DE 15 59196381 59196381 deletion of <=200bp T - intron_variant PBCA-DE 15 59204647 59204647 single base substitution A C intron_variant PBCA-DE 15 59205148 59205148 single base substitution T C intron_variant PBCA-DE 15 59219431 59219431 insertion of <=200bp - T intron_variant PBCA-DE 15 59227766 59227766 insertion of <=200bp - T intron_variant PBCA-DE 15 59239126 59239127 deletion of <=200bp TG - intron_variant PBCA-DE 15 59240452 59240467 deletion of <=200bp GGTCAAAATGGAAAGC - intron_variant PBCA-DE 15 59240486 59240486 deletion of <=200bp T - intron_variant PBCA-DE 15 59246916 59246916 single base substitution G A intron_variant PBCA-DE 15 59249882 59249883 deletion of <=200bp GA - intron_variant PBCA-DE 15 59252743 59252743 single base substitution G A intron_variant PBCA-DE 15 59252984 59252984 single base substitution C T intron_variant PBCA-DE 15 59256287 59256287 single base substitution C G intron_variant PBCA-DE 15 59264216 59264216 single base substitution C T intron_variant PBCA-DE 15 59274737 59274737 single base substitution G A intron_variant PBCA-DE 15 59293104 59293104 single base substitution G A intron_variant PBCA-DE 15 59301147 59301147 single base substitution G A intron_variant PBCA-DE 15 59325089 59325090 deletion of <=200bp CT - downstream_gene_variant PBCA-DE 15 59325089 59325090 deletion of <=200bp CT - intron_variant PBCA-DE 15 59333972 59333972 single base substitution T C intron_variant PBCA-DE 15 59341552 59341552 single base substitution G A intron_variant PBCA-DE 15 59345371 59345371 single base substitution G A intron_variant PBCA-DE 15 59350845 59350845 insertion of <=200bp - GG 3_prime_UTR_variant PBCA-DE 15 59350845 59350845 insertion of <=200bp - GG intron_variant PBCA-DE 15 59355564 59355564 single base substitution T A downstream_gene_variant PBCA-DE 15 59355564 59355564 single base substitution T A intron_variant PBCA-DE 15 59359357 59359357 single base substitution C T intron_variant PBCA-DE 15 59362220 59362220 single base substitution A C intron_variant PBCA-DE 15 59362226 59362226 single base substitution T C intron_variant PBCA-DE 15 59365537 59365537 insertion of <=200bp - CT intron_variant PBCA-DE 15 59377330 59377330 single base substitution A T downstream_gene_variant PBCA-DE 15 59377330 59377330 single base substitution A T intron_variant PBCA-DE 15 59377330 59377330 single base substitution A T upstream_gene_variant PBCA-DE 15 59390247 59390248 deletion of <=200bp AC - downstream_gene_variant PRAD-CA 15 59180690 59180690 single base substitution G A intron_variant PRAD-CA 15 59190848 59190848 single base substitution A C intron_variant PRAD-CA 15 59196041 59196041 single base substitution G A intron_variant PRAD-CA 15 59230683 59230683 single base substitution T A intron_variant PRAD-CA 15 59253708 59253708 single base substitution G C intron_variant PRAD-CA 15 59254174 59254174 single base substitution A C intron_variant PRAD-CA 15 59257531 59257531 single base substitution A G intron_variant PRAD-CA 15 59261801 59261801 single base substitution C G intron_variant PRAD-CA 15 59274509 59274509 single base substitution T C intron_variant PRAD-CA 15 59279009 59279009 single base substitution C T intron_variant PRAD-CA 15 59279009 59279009 single base substitution C T upstream_gene_variant PRAD-CA 15 59284685 59284685 single base substitution C A intron_variant PRAD-CA 15 59298303 59298303 single base substitution A C intron_variant PRAD-CA 15 59305878 59305878 single base substitution G T intron_variant PRAD-CA 15 59341827 59341827 single base substitution T C intron_variant PRAD-CA 15 59369274 59369274 single base substitution T G intron_variant PRAD-CA 15 59369274 59369274 single base substitution T G upstream_gene_variant PRAD-CA 15 59371596 59371596 single base substitution G C intron_variant PRAD-CA 15 59371596 59371596 single base substitution G C upstream_gene_variant PRAD-CA 15 59394044 59394044 single base substitution A G downstream_gene_variant PRAD-UK 15 59160809 59160809 single base substitution A G intron_variant PRAD-UK 15 59160814 59160814 single base substitution G A intron_variant PRAD-UK 15 59166478 59166478 deletion of <=200bp C - intron_variant PRAD-UK 15 59193494 59193494 single base substitution T C intron_variant PRAD-UK 15 59217139 59217139 single base substitution C G intron_variant PRAD-UK 15 59230907 59230907 single base substitution G C intron_variant PRAD-UK 15 59231720 59231720 single base substitution G A intron_variant PRAD-UK 15 59245979 59245979 single base substitution T A intron_variant PRAD-UK 15 59268592 59268592 single base substitution T C intron_variant PRAD-UK 15 59276496 59276496 single base substitution C T intron_variant PRAD-UK 15 59276496 59276496 single base substitution C T upstream_gene_variant PRAD-UK 15 59311752 59311752 single base substitution C G intron_variant PRAD-UK 15 59319842 59319842 single base substitution G A intron_variant PRAD-UK 15 59319842 59319842 single base substitution G A upstream_gene_variant PRAD-UK 15 59329357 59329357 single base substitution G A intron_variant PRAD-UK 15 59332316 59332316 single base substitution T A intron_variant PRAD-UK 15 59333718 59333718 single base substitution C T intron_variant PRAD-UK 15 59361010 59361010 single base substitution T G intron_variant PRAD-UK 15 59382111 59382111 single base substitution T C downstream_gene_variant PRAD-UK 15 59382111 59382111 single base substitution T C intron_variant PRAD-UK 15 59382111 59382111 single base substitution T C upstream_gene_variant PRAD-US 15 59179240 59179240 single base substitution G A intron_variant PRAD-US 15 59182525 59182526 deletion of <=200bp TC - intron_variant READ-US 15 59323719 59323719 single base substitution T G downstream_gene_variant READ-US 15 59323719 59323719 single base substitution T G stop_gained L233* 698T>G READ-US 15 59323719 59323719 single base substitution T G upstream_gene_variant READ-US 15 59359251 59359251 single base substitution A C missense_variant N552T 1655A>C RECA-EU 15 59157566 59157566 single base substitution G T intron_variant RECA-EU 15 59157567 59157567 single base substitution C A intron_variant RECA-EU 15 59165733 59165733 single base substitution T C intron_variant RECA-EU 15 59212572 59212572 single base substitution C T intron_variant RECA-EU 15 59228089 59228089 single base substitution T C intron_variant RECA-EU 15 59233630 59233630 single base substitution A G intron_variant RECA-EU 15 59239353 59239353 single base substitution A G intron_variant RECA-EU 15 59241914 59241914 single base substitution G A intron_variant RECA-EU 15 59270712 59270712 single base substitution T A intron_variant RECA-EU 15 59273842 59273842 single base substitution G T intron_variant RECA-EU 15 59274486 59274486 single base substitution T A intron_variant RECA-EU 15 59305118 59305118 single base substitution A T intron_variant RECA-EU 15 59306333 59306333 single base substitution T G intron_variant RECA-EU 15 59313710 59313710 single base substitution G A intron_variant RECA-EU 15 59317854 59317854 single base substitution A T intron_variant RECA-EU 15 59347147 59347147 single base substitution C T intron_variant RECA-EU 15 59351948 59351948 single base substitution C G downstream_gene_variant RECA-EU 15 59351948 59351948 single base substitution C G intron_variant RECA-EU 15 59364726 59364726 single base substitution C A intron_variant RECA-EU 15 59374409 59374409 single base substitution T A intron_variant RECA-EU 15 59374409 59374409 single base substitution T A upstream_gene_variant RECA-EU 15 59376983 59376983 single base substitution C A downstream_gene_variant RECA-EU 15 59376983 59376983 single base substitution C A intron_variant RECA-EU 15 59376983 59376983 single base substitution C A upstream_gene_variant RECA-EU 15 59387561 59387561 single base substitution T C 3_prime_UTR_variant RECA-EU 15 59387561 59387561 single base substitution T C downstream_gene_variant RECA-EU 15 59387561 59387561 single base substitution T C exon_variant SKCA-BR 15 59155217 59155218 deletion of <=200bp GT - upstream_gene_variant SKCA-BR 15 59155252 59155252 single base substitution A G upstream_gene_variant SKCA-BR 15 59157257 59157257 single base substitution C T upstream_gene_variant SKCA-BR 15 59160188 59160188 single base substitution A G intron_variant SKCA-BR 15 59172179 59172179 single base substitution C T intron_variant SKCA-BR 15 59172508 59172508 single base substitution T C intron_variant SKCA-BR 15 59174282 59174282 single base substitution T C intron_variant SKCA-BR 15 59183646 59183646 single base substitution T C intron_variant SKCA-BR 15 59185956 59185956 single base substitution C T intron_variant SKCA-BR 15 59188211 59188211 single base substitution G A intron_variant SKCA-BR 15 59192257 59192258 deletion of <=200bp GA - intron_variant SKCA-BR 15 59197422 59197422 single base substitution G A intron_variant SKCA-BR 15 59199818 59199824 deletion of <=200bp TCAACAA - intron_variant SKCA-BR 15 59208199 59208199 single base substitution T A intron_variant SKCA-BR 15 59212111 59212111 single base substitution G A intron_variant SKCA-BR 15 59212826 59212826 insertion of <=200bp - TAATA intron_variant SKCA-BR 15 59213808 59213808 single base substitution G A intron_variant SKCA-BR 15 59214736 59214747 deletion of <=200bp ATATTTTATATG - intron_variant SKCA-BR 15 59218177 59218177 single base substitution G A intron_variant SKCA-BR 15 59221438 59221438 single base substitution T G intron_variant SKCA-BR 15 59222572 59222572 single base substitution A C intron_variant SKCA-BR 15 59226043 59226043 single base substitution T G intron_variant SKCA-BR 15 59227892 59227892 single base substitution A C intron_variant SKCA-BR 15 59228088 59228088 insertion of <=200bp - TC intron_variant SKCA-BR 15 59229944 59229944 single base substitution G A intron_variant SKCA-BR 15 59230467 59230467 single base substitution C T intron_variant SKCA-BR 15 59231221 59231221 single base substitution A G intron_variant SKCA-BR 15 59233523 59233523 single base substitution G A intron_variant SKCA-BR 15 59233993 59233993 single base substitution C T intron_variant SKCA-BR 15 59234323 59234323 single base substitution T C intron_variant SKCA-BR 15 59235535 59235535 single base substitution T G intron_variant SKCA-BR 15 59236295 59236295 single base substitution C T intron_variant SKCA-BR 15 59236598 59236606 deletion of <=200bp AATTTATTT - intron_variant SKCA-BR 15 59236719 59236719 single base substitution A T intron_variant SKCA-BR 15 59237055 59237055 insertion of <=200bp - GA intron_variant SKCA-BR 15 59237057 59237057 single base substitution T A intron_variant SKCA-BR 15 59241319 59241319 single base substitution T C intron_variant SKCA-BR 15 59241547 59241547 single base substitution G A intron_variant SKCA-BR 15 59242655 59242655 single base substitution C T intron_variant SKCA-BR 15 59249977 59249977 single base substitution A G intron_variant SKCA-BR 15 59252337 59252337 single base substitution G A intron_variant SKCA-BR 15 59252751 59252751 single base substitution C T intron_variant SKCA-BR 15 59254973 59254973 single base substitution C T intron_variant SKCA-BR 15 59255873 59255873 single base substitution G A intron_variant SKCA-BR 15 59256937 59256937 single base substitution A C intron_variant SKCA-BR 15 59260665 59260665 single base substitution A C intron_variant SKCA-BR 15 59260728 59260728 single base substitution A G intron_variant SKCA-BR 15 59262700 59262700 single base substitution C A intron_variant SKCA-BR 15 59263200 59263200 single base substitution A T intron_variant SKCA-BR 15 59263677 59263677 single base substitution C T intron_variant SKCA-BR 15 59264721 59264722 deletion of <=200bp CT - intron_variant SKCA-BR 15 59265467 59265467 single base substitution T G intron_variant SKCA-BR 15 59269090 59269090 insertion of <=200bp - AAATAT intron_variant SKCA-BR 15 59269124 59269124 single base substitution T C intron_variant SKCA-BR 15 59269572 59269572 single base substitution C T intron_variant SKCA-BR 15 59270890 59270890 single base substitution A C intron_variant SKCA-BR 15 59274454 59274457 deletion of <=200bp AGTC - intron_variant SKCA-BR 15 59274455 59274455 insertion of <=200bp - GTCTTCTTCTTCTTCTTCTTCT intron_variant SKCA-BR 15 59274455 59274455 insertion of <=200bp - GTCTTCTTCTTCTTCTTCTTCTTCT intron_variant SKCA-BR 15 59274458 59274458 single base substitution G T intron_variant SKCA-BR 15 59274465 59274465 single base substitution T A intron_variant SKCA-BR 15 59274486 59274486 single base substitution T A intron_variant SKCA-BR 15 59274489 59274489 single base substitution T A intron_variant SKCA-BR 15 59274509 59274509 insertion of <=200bp - TTCTTCTTCTTCTTCC intron_variant SKCA-BR 15 59278184 59278184 single base substitution G C intron_variant SKCA-BR 15 59278184 59278184 single base substitution G C upstream_gene_variant SKCA-BR 15 59283286 59283286 single base substitution T G intron_variant SKCA-BR 15 59283339 59283339 single base substitution T A intron_variant SKCA-BR 15 59284003 59284003 single base substitution G A intron_variant SKCA-BR 15 59286232 59286232 insertion of <=200bp - AT intron_variant SKCA-BR 15 59286672 59286673 deletion of <=200bp CT - intron_variant SKCA-BR 15 59287963 59287964 deletion of <=200bp CT - intron_variant SKCA-BR 15 59287996 59287996 single base substitution C T intron_variant SKCA-BR 15 59289715 59289716 deletion of <=200bp TA - intron_variant SKCA-BR 15 59299364 59299364 single base substitution C T intron_variant SKCA-BR 15 59301169 59301169 single base substitution A T intron_variant SKCA-BR 15 59310154 59310154 single base substitution C T intron_variant SKCA-BR 15 59311304 59311305 deletion of <=200bp AT - intron_variant SKCA-BR 15 59316038 59316038 single base substitution C A intron_variant SKCA-BR 15 59320629 59320629 single base substitution T G intron_variant SKCA-BR 15 59320629 59320629 single base substitution T G upstream_gene_variant SKCA-BR 15 59325790 59325790 single base substitution C T downstream_gene_variant SKCA-BR 15 59325790 59325790 single base substitution C T intron_variant SKCA-BR 15 59337992 59337992 single base substitution C T intron_variant SKCA-BR 15 59339492 59339492 single base substitution C T intron_variant SKCA-BR 15 59341908 59341908 single base substitution C T intron_variant SKCA-BR 15 59341944 59341944 insertion of <=200bp - CT intron_variant SKCA-BR 15 59343990 59343990 single base substitution A G intron_variant SKCA-BR 15 59344757 59344757 single base substitution C T intron_variant SKCA-BR 15 59353006 59353006 insertion of <=200bp - ATTT downstream_gene_variant SKCA-BR 15 59353006 59353006 insertion of <=200bp - ATTT intron_variant SKCA-BR 15 59354746 59354746 single base substitution G A downstream_gene_variant SKCA-BR 15 59354746 59354746 single base substitution G A intron_variant SKCA-BR 15 59356850 59356850 single base substitution C T intron_variant SKCA-BR 15 59357893 59357893 single base substitution G A intron_variant SKCA-BR 15 59359453 59359453 single base substitution T A intron_variant SKCA-BR 15 59362202 59362202 single base substitution A C intron_variant SKCA-BR 15 59362209 59362209 single base substitution A C intron_variant SKCA-BR 15 59363968 59363968 single base substitution C T intron_variant SKCA-BR 15 59364014 59364014 single base substitution G A intron_variant SKCA-BR 15 59370371 59370371 single base substitution C T intron_variant SKCA-BR 15 59370371 59370371 single base substitution C T upstream_gene_variant SKCA-BR 15 59379333 59379333 single base substitution C T downstream_gene_variant SKCA-BR 15 59379333 59379333 single base substitution C T intron_variant SKCA-BR 15 59385560 59385560 insertion of <=200bp - TC downstream_gene_variant SKCA-BR 15 59385560 59385560 insertion of <=200bp - TC intron_variant SKCA-BR 15 59385560 59385560 insertion of <=200bp - TC upstream_gene_variant SKCA-BR 15 59385560 59385560 insertion of <=200bp - TTC downstream_gene_variant SKCA-BR 15 59385560 59385560 insertion of <=200bp - TTC intron_variant SKCA-BR 15 59385560 59385560 insertion of <=200bp - TTC upstream_gene_variant SKCA-BR 15 59385560 59385560 single base substitution T C downstream_gene_variant SKCA-BR 15 59385560 59385560 single base substitution T C intron_variant SKCA-BR 15 59385560 59385560 single base substitution T C upstream_gene_variant SKCA-BR 15 59385561 59385561 single base substitution C T downstream_gene_variant SKCA-BR 15 59385561 59385561 single base substitution C T intron_variant SKCA-BR 15 59385561 59385561 single base substitution C T upstream_gene_variant SKCA-BR 15 59385747 59385747 single base substitution C T downstream_gene_variant SKCA-BR 15 59385747 59385747 single base substitution C T intron_variant SKCA-BR 15 59386134 59386134 single base substitution G A downstream_gene_variant SKCA-BR 15 59386134 59386134 single base substitution G A intron_variant SKCA-BR 15 59390846 59390847 deletion of <=200bp TA - downstream_gene_variant SKCA-BR 15 59391836 59391836 single base substitution G A downstream_gene_variant SKCA-BR 15 59392911 59392913 deletion of <=200bp AAG - downstream_gene_variant SKCA-BR 15 59393951 59393968 deletion of <=200bp AGAATCACTTGAACCTGG - downstream_gene_variant SKCM-US 15 59179248 59179248 single base substitution G A intron_variant SKCM-US 15 59179506 59179506 single base substitution G A intron_variant SKCM-US 15 59179516 59179516 single base substitution G A intron_variant SKCM-US 15 59179696 59179696 single base substitution G A intron_variant SKCM-US 15 59180621 59180621 single base substitution G A intron_variant SKCM-US 15 59180636 59180636 single base substitution C T intron_variant SKCM-US 15 59180640 59180640 single base substitution G A intron_variant SKCM-US 15 59182564 59182565 deletion of <=200bp CT - intron_variant SKCM-US 15 59182605 59182605 single base substitution G A intron_variant SKCM-US 15 59192026 59192026 single base substitution T G intron_variant SKCM-US 15 59323125 59323125 single base substitution G A missense_variant G35E 104G>A SKCM-US 15 59323125 59323125 single base substitution G A missense_variant G58E 173G>A SKCM-US 15 59323125 59323125 single base substitution G A upstream_gene_variant SKCM-US 15 59323751 59323751 single base substitution C T downstream_gene_variant SKCM-US 15 59323751 59323751 single base substitution C T stop_gained R244* 730C>T SKCM-US 15 59323751 59323751 single base substitution C T upstream_gene_variant SKCM-US 15 59323895 59323895 single base substitution C T downstream_gene_variant SKCM-US 15 59323895 59323895 single base substitution C T missense_variant P25S 73C>T SKCM-US 15 59323895 59323895 single base substitution C T missense_variant P292S 874C>T SKCM-US 15 59359153 59359153 single base substitution C T synonymous_variant H519H 1557C>T SKCM-US 15 59373179 59373179 single base substitution C T exon_variant SKCM-US 15 59373179 59373179 single base substitution C T missense_variant P665S 1993C>T SKCM-US 15 59373179 59373179 single base substitution C T upstream_gene_variant SKCM-US 15 59373233 59373233 single base substitution T C exon_variant SKCM-US 15 59373233 59373233 single base substitution T C missense_variant Y683H 2047T>C SKCM-US 15 59373233 59373233 single base substitution T C upstream_gene_variant SKCM-US 15 59373248 59373248 single base substitution C T exon_variant SKCM-US 15 59373248 59373248 single base substitution C T missense_variant P688S 2062C>T SKCM-US 15 59373248 59373248 single base substitution C T upstream_gene_variant SKCM-US 15 59373274 59373274 single base substitution A T exon_variant SKCM-US 15 59373274 59373274 single base substitution A T synonymous_variant I696I 2088A>T SKCM-US 15 59373274 59373274 single base substitution A T upstream_gene_variant SKCM-US 15 59373296 59373296 single base substitution C T exon_variant SKCM-US 15 59373296 59373296 single base substitution C T missense_variant P704S 2110C>T SKCM-US 15 59373296 59373296 single base substitution C T upstream_gene_variant SKCM-US 15 59381920 59381920 single base substitution G C downstream_gene_variant SKCM-US 15 59381920 59381920 single base substitution G C exon_variant SKCM-US 15 59381920 59381920 single base substitution G C missense_variant G869R 2605G>C SKCM-US 15 59381920 59381920 single base substitution G C missense_variant G878R 2632G>C SKCM-US 15 59381920 59381920 single base substitution G C upstream_gene_variant SKCM-US 15 59383267 59383267 single base substitution C T downstream_gene_variant SKCM-US 15 59383267 59383267 single base substitution C T exon_variant SKCM-US 15 59383267 59383267 single base substitution C T missense_variant H885Y 2653C>T SKCM-US 15 59383267 59383267 single base substitution C T missense_variant H894Y 2680C>T SKCM-US 15 59383267 59383267 single base substitution C T upstream_gene_variant STAD-US 15 59180672 59180672 single base substitution G A intron_variant STAD-US 15 59181683 59181683 single base substitution C T intron_variant STAD-US 15 59181694 59181694 single base substitution T C intron_variant STAD-US 15 59181732 59181732 single base substitution G A intron_variant STAD-US 15 59182562 59182562 single base substitution C T intron_variant STAD-US 15 59182634 59182634 single base substitution C T intron_variant STAD-US 15 59182636 59182637 deletion of <=200bp CT - intron_variant STAD-US 15 59185211 59185211 deletion of <=200bp T - intron_variant STAD-US 15 59186099 59186099 single base substitution A G intron_variant STAD-US 15 59186117 59186117 single base substitution A G intron_variant STAD-US 15 59186298 59186298 single base substitution C T intron_variant STAD-US 15 59186705 59186705 single base substitution C T intron_variant STAD-US 15 59191666 59191666 single base substitution A G intron_variant STAD-US 15 59192084 59192084 single base substitution T C intron_variant STAD-US 15 59323599 59323599 single base substitution C T downstream_gene_variant STAD-US 15 59323599 59323599 single base substitution C T missense_variant S193L 578C>T STAD-US 15 59323599 59323599 single base substitution C T upstream_gene_variant STAD-US 15 59323672 59323672 insertion of <=200bp - A downstream_gene_variant STAD-US 15 59323672 59323672 insertion of <=200bp - A frameshift_variant V217V? STAD-US 15 59323672 59323672 insertion of <=200bp - A upstream_gene_variant STAD-US 15 59347967 59347967 single base substitution G A missense_variant R365H 1094G>A STAD-US 15 59347967 59347967 single base substitution G A missense_variant R98H 293G>A STAD-US 15 59359012 59359012 single base substitution T C synonymous_variant P472P 1416T>C STAD-US 15 59368267 59368267 single base substitution A G missense_variant I601V 1801A>G STAD-US 15 59368267 59368267 single base substitution A G upstream_gene_variant STAD-US 15 59373146 59373146 single base substitution A G exon_variant STAD-US 15 59373146 59373146 single base substitution A G missense_variant T654A 1960A>G STAD-US 15 59373146 59373146 single base substitution A G upstream_gene_variant STAD-US 15 59373169 59373169 single base substitution T C exon_variant STAD-US 15 59373169 59373169 single base substitution T C synonymous_variant A661A 1983T>C STAD-US 15 59373169 59373169 single base substitution T C upstream_gene_variant STAD-US 15 59373220 59373220 single base substitution G A exon_variant STAD-US 15 59373220 59373220 single base substitution G A synonymous_variant P678P 2034G>A STAD-US 15 59373220 59373220 single base substitution G A upstream_gene_variant STAD-US 15 59376343 59376343 deletion of <=200bp C - exon_variant STAD-US 15 59376343 59376343 deletion of <=200bp C - frameshift_variant R771 STAD-US 15 59376343 59376343 deletion of <=200bp C - frameshift_variant R780 STAD-US 15 59376343 59376343 deletion of <=200bp C - upstream_gene_variant STAD-US 15 59381897 59381897 single base substitution G A downstream_gene_variant STAD-US 15 59381897 59381897 single base substitution G A exon_variant STAD-US 15 59381897 59381897 single base substitution G A missense_variant R861H 2582G>A STAD-US 15 59381897 59381897 single base substitution G A missense_variant R870H 2609G>A STAD-US 15 59381897 59381897 single base substitution G A upstream_gene_variant THCA-SA 15 59323048 59323048 single base substitution C G missense_variant N32K 96C>G THCA-SA 15 59323048 59323048 single base substitution C G missense_variant N9K 27C>G THCA-SA 15 59323048 59323048 single base substitution C G upstream_gene_variant UCEC-US 15 59175970 59175970 single base substitution G A intron_variant UCEC-US 15 59180619 59180619 single base substitution A G intron_variant UCEC-US 15 59180686 59180686 single base substitution C T intron_variant UCEC-US 15 59180747 59180747 single base substitution C A intron_variant UCEC-US 15 59181746 59181746 single base substitution C T intron_variant UCEC-US 15 59182496 59182496 single base substitution C T intron_variant UCEC-US 15 59182564 59182565 deletion of <=200bp CT - intron_variant UCEC-US 15 59182632 59182632 single base substitution G A intron_variant UCEC-US 15 59185115 59185115 single base substitution G A intron_variant UCEC-US 15 59185137 59185137 single base substitution T G intron_variant UCEC-US 15 59185145 59185145 single base substitution C T intron_variant UCEC-US 15 59185179 59185179 single base substitution C T intron_variant UCEC-US 15 59186051 59186051 single base substitution C T intron_variant UCEC-US 15 59186128 59186128 single base substitution C A intron_variant UCEC-US 15 59186159 59186159 single base substitution C A intron_variant UCEC-US 15 59186698 59186699 deletion of <=200bp CT - intron_variant UCEC-US 15 59186750 59186750 single base substitution C T intron_variant UCEC-US 15 59205829 59205829 single base substitution C A intron_variant UCEC-US 15 59205860 59205860 single base substitution T G intron_variant UCEC-US 15 59323277 59323277 single base substitution G T stop_gained E109* 325G>T UCEC-US 15 59323277 59323277 single base substitution G T stop_gained E86* 256G>T UCEC-US 15 59323277 59323277 single base substitution G T upstream_gene_variant UCEC-US 15 59323499 59323499 single base substitution G T downstream_gene_variant UCEC-US 15 59323499 59323499 single base substitution G T stop_gained E160* 478G>T UCEC-US 15 59323499 59323499 single base substitution G T upstream_gene_variant UCEC-US 15 59323665 59323665 single base substitution G T downstream_gene_variant UCEC-US 15 59323665 59323665 single base substitution G T missense_variant R215I 644G>T UCEC-US 15 59323665 59323665 single base substitution G T upstream_gene_variant UCEC-US 15 59323676 59323676 single base substitution A C downstream_gene_variant UCEC-US 15 59323676 59323676 single base substitution A C missense_variant N219H 655A>C UCEC-US 15 59323676 59323676 single base substitution A C upstream_gene_variant UCEC-US 15 59323816 59323816 single base substitution C A downstream_gene_variant UCEC-US 15 59323816 59323816 single base substitution C A synonymous_variant S265S 795C>A UCEC-US 15 59323816 59323816 single base substitution C A upstream_gene_variant UCEC-US 15 59323858 59323858 single base substitution T C downstream_gene_variant UCEC-US 15 59323858 59323858 single base substitution T C synonymous_variant V12V 36T>C UCEC-US 15 59323858 59323858 single base substitution T C synonymous_variant V279V 837T>C UCEC-US 15 59344571 59344571 single base substitution A C missense_variant E316D 948A>C UCEC-US 15 59344571 59344571 single base substitution A C missense_variant E49D 147A>C UCEC-US 15 59344632 59344632 single base substitution T C splice_donor_variant UCEC-US 15 59347881 59347881 single base substitution G A splice_region_variant UCEC-US 15 59350735 59350735 single base substitution G A missense_variant G184D 551G>A UCEC-US 15 59350735 59350735 single base substitution G A missense_variant G451D 1352G>A UCEC-US 15 59359083 59359083 single base substitution C T missense_variant A496V 1487C>T UCEC-US 15 59359127 59359127 single base substitution C T missense_variant H511Y 1531C>T UCEC-US 15 59359263 59359263 single base substitution G A missense_variant G556D 1667G>A UCEC-US 15 59368377 59368380 deletion of <=200bp CTCT - frameshift_variant PS637 UCEC-US 15 59368377 59368380 deletion of <=200bp CTCT - upstream_gene_variant UCEC-US 15 59373219 59373219 single base substitution C T exon_variant UCEC-US 15 59373219 59373219 single base substitution C T missense_variant P678L 2033C>T UCEC-US 15 59373219 59373219 single base substitution C T upstream_gene_variant UCEC-US 15 59373373 59373373 single base substitution G T exon_variant UCEC-US 15 59373373 59373373 single base substitution G T missense_variant Q729H 2187G>T UCEC-US 15 59373373 59373373 single base substitution G T upstream_gene_variant UCEC-US 15 59376433 59376433 single base substitution G A exon_variant UCEC-US 15 59376433 59376433 single base substitution G A synonymous_variant Q801Q 2403G>A UCEC-US 15 59376433 59376433 single base substitution G A synonymous_variant Q810Q 2430G>A UCEC-US 15 59376433 59376433 single base substitution G A upstream_gene_variant UCEC-US 15 59377946 59377946 single base substitution C T downstream_gene_variant UCEC-US 15 59377946 59377946 single base substitution C T exon_variant UCEC-US 15 59377946 59377946 single base substitution C T stop_gained R838* 2512C>T UCEC-US 15 59377946 59377946 single base substitution C T stop_gained R847* 2539C>T UCEC-US 15 59383284 59383284 single base substitution A C downstream_gene_variant UCEC-US 15 59383284 59383284 single base substitution A C exon_variant UCEC-US 15 59383284 59383284 single base substitution A C missense_variant L890F 2670A>C UCEC-US 15 59383284 59383284 single base substitution A C missense_variant L899F 2697A>C UCEC-US 15 59383284 59383284 single base substitution A C upstream_gene_variant UCEC-US 15 59384797 59384797 single base substitution G T downstream_gene_variant UCEC-US 15 59384797 59384797 single base substitution G T exon_variant UCEC-US 15 59384797 59384797 single base substitution G T missense_variant C934F 2801G>T UCEC-US 15 59384797 59384797 single base substitution G T missense_variant C942F 2825G>T UCEC-US 15 59384797 59384797 single base substitution G T missense_variant C943F 2828G>T UCEC-US 15 59384797 59384797 single base substitution G T missense_variant C951F 2852G>T UCEC-US 15 59384797 59384797 single base substitution G T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand BD236T COSM5519313 c.602G>T p.C201F Substitution - Missense 15:59031424-59031424 + TCGA-FW-A3R5-06 COSM3887265 c.1993C>T p.P665S Substitution - Missense 15:59080980-59080980 + TCGA-AM-5820-01 COSM3754377 c.27C>G p.N9K Substitution - Missense 15:59030849-59030849 + RK337_C01 COSM1749240 c.2687G>A p.G896E Substitution - Missense 15:59091102-59091102 + 228 COSM963405 c.2187G>T p.Q729H Substitution - Missense 15:59081174-59081174 + TCGA-BR-4361-01 COSM1264333 c.2034G>A p.P678P Substitution - coding silent 15:59081021-59081021 + TCGA-36-2548-01 COSM1323922 c.1007+1G>T p.? Unknown 15:59052432-59052432 + CSCC-31-T COSM4477671 c.2173C>T p.P725S Substitution - Missense 15:59081160-59081160 + TCGA-CA-6717-01 COSM1373807 c.2848C>A p.L950I Substitution - Missense 15:59094787-59094787 + TCGA-DK-A1A3-01 COSM416878 c.892G>A p.E298K Substitution - Missense 15:59052316-59052316 + TCGA-AX-A0J1-01 COSM963401 c.1667G>A p.G556D Substitution - Missense 15:59067064-59067064 + 8033510 COSM3386964 c.1612C>G p.P538A Substitution - Missense 15:59067009-59067009 + 01-P034 COSM1478223 c.1337_1351del15 p.N447_G451delNSTTG Deletion - In frame 15:59058521-59058535 + ESO-708 COSM295676 c.1792C>T p.R598* Substitution - Nonsense 15:59076059-59076059 + T3024 COSM4721932 c.1881G>A p.A627A Substitution - coding silent 15:59076148-59076148 + ESCC_16 COSM5625764 c.2020C>G p.Q674E Substitution - Missense 15:59081007-59081007 + T3336 COSM295676 c.1792C>T p.R598* Substitution - Nonsense 15:59076059-59076059 + TCGA-EB-A44N-01 COSM3502789 c.2088A>T p.I696I Substitution - coding silent 15:59081075-59081075 + TCGA-E9-A243-01 COSM1478221 c.128T>A p.I43N Substitution - Missense 15:59030950-59030950 + 1739 COSM213699 c.2705T>C p.I902T Substitution - Missense 15:59091120-59091120 + LIM2405 COSM4641939 c.1909C>T p.P637S Substitution - Missense 15:59076176-59076176 + YURUS COSM1373801 c.2683C>T p.R895C Substitution - Missense 15:59091098-59091098 + I2L-P31-Tumor-Organoid COSM5363048 c.1606G>T p.A536S Substitution - Missense 15:59067003-59067003 + HCC2998 COSM2219663 c.2187G>C p.Q729H Substitution - Missense 15:59081174-59081174 + CSCC-40-T COSM4449604 c.277delA p.K94fs*23 Deletion - Frameshift 15:59031099-59031099 + GHE0645 COSM5714596 c.2953G>A p.E985K Substitution - Missense 15:59094892-59094892 + TCGA-A6-6781-01 COSM1373799 c.2313delC p.P773fs*44 Deletion - Frameshift 15:59084144-59084144 + KM12 COSM2219593 c.352C>T p.L118L Substitution - coding silent 15:59031174-59031174 + TCGA-AC-A2BK-01 COSM3816451 c.1027C>T p.H343Y Substitution - Missense 15:59055701-59055701 + TCGA-66-2773-01 COSM700840 c.2038C>G p.Q680E Substitution - Missense 15:59081025-59081025 + AA1924 COSM4168895 c.2801G>A p.C934Y Substitution - Missense 15:59092598-59092598 + HCC66 COSM1608518 c.250G>T p.E84* Substitution - Nonsense 15:59031072-59031072 + HCC127 COSM3706651 c.2740-5C>A p.? Unknown 15:59092532-59092532 + TCGA-18-3409-01 COSM700838 c.2177C>T p.P726L Substitution - Missense 15:59081164-59081164 + 081T COSM1730815 c.1679A>T p.H560L Substitution - Missense 15:59067076-59067076 + TCGA-EI-6917-01 COSM3420482 c.1655A>C p.N552T Substitution - Missense 15:59067052-59067052 + 37 COSM5733621 c.1850C>T p.S617L Substitution - Missense 15:59076117-59076117 + B59-3-Tumor COSM1749240 c.2687G>A p.G896E Substitution - Missense 15:59091102-59091102 + TCGA-EE-A2GJ-06 COSM3502781 c.104G>A p.G35E Substitution - Missense 15:59030926-59030926 + 2292380 COSM4610005 c.1915C>A p.L639I Substitution - Missense 15:59076182-59076182 + TCGA-D1-A0ZZ-01 COSM963389 c.1007+2T>C p.? Unknown 15:59052433-59052433 + BD236T COSM5519315 c.2297+5G>T p.? Unknown 15:59081289-59081289 + TCGA-AG-3892-01 COSM257901 c.1681G>T p.E561* Substitution - Nonsense 15:59067078-59067078 + TCGA-A5-A0GD-01 COSM963393 c.1300C>A p.P434T Substitution - Missense 15:59058484-59058484 + GC1_T COSM3748599 c.1978C>T p.Q660* Substitution - Nonsense 15:59080965-59080965 + TCGA-A8-A09Z-01 COSM5202368 c.1569delC p.P524fs*46 Deletion - Frameshift 15:59066966-59066966 + pfg016T COSM1640306 c.2734delA p.K913fs*29 Deletion - Frameshift 15:59091149-59091149 + TCGA-D9-A6EC-06 COSM4401591 c.2062C>T p.P688S Substitution - Missense 15:59081049-59081049 + TCGA-AM-5821-01 COSM1179761 c.1056C>A p.S352S Substitution - coding silent 15:59055730-59055730 + SA102 COSM213699 c.2705T>C p.I902T Substitution - Missense 15:59091120-59091120 + CSCC-56-T COSM4504346 c.662C>T p.S221F Substitution - Missense 15:59031484-59031484 + ESCC_BICR_038T COSM5434520 c.1917C>G p.L639L Substitution - coding silent 15:59076184-59076184 + TCGA-CW-5589-01 COSM470888 c.2311C>T p.R771C Substitution - Missense 15:59084142-59084142 + SWE-37 COSM1179761 c.1056C>A p.S352S Substitution - coding silent 15:59055730-59055730 + B52-Tumor COSM1749238 c.2424G>C p.W808C Substitution - Missense 15:59085659-59085659 + HCC66T COSM1608518 c.250G>T p.E84* Substitution - Nonsense 15:59031072-59031072 + TCGA-BS-A0UV-01 COSM963413 c.2801G>T p.C934F Substitution - Missense 15:59092598-59092598 + LS411 COSM2219631 c.1724G>T p.R575I Substitution - Missense 15:59075991-59075991 + ACC-2 COSM4967759 c.1992C>A p.C664* Substitution - Nonsense 15:59080979-59080979 + TCGA-B5-A11E-01 COSM963411 c.2670A>C p.L890F Substitution - Missense 15:59091085-59091085 + 462 COSM3502783 c.730C>T p.R244* Substitution - Nonsense 15:59031552-59031552 + TCGA-A5-A0VO-01 COSM963399 c.1531C>T p.H511Y Substitution - Missense 15:59066928-59066928 + T660 COSM4721930 c.1819G>A p.A607T Substitution - Missense 15:59076086-59076086 + PTC-7C COSM3754377 c.27C>G p.N9K Substitution - Missense 15:59030849-59030849 + TCGA-G2-A2EF-01 COSM1301265 c.1268C>T p.S423F Substitution - Missense 15:59058452-59058452 + PCSI_0017_Pa_X COSM3377603 c.1255T>C p.S419P Substitution - Missense 15:59058439-59058439 + TCGA-AX-A0J0-01 COSM963375 c.256G>T p.E86* Substitution - Nonsense 15:59031078-59031078 + TCGA-G2-A3VY-01 COSM3794271 c.758C>G p.S253C Substitution - Missense 15:59031580-59031580 + TCGA-AX-A05Z-01 COSM963379 c.644G>T p.R215I Substitution - Missense 15:59031466-59031466 + I2L-P31-Tumor-Biopsy COSM5363048 c.1606G>T p.A536S Substitution - Missense 15:59067003-59067003 + SNUH_G37_S1 COSM3678232 c.1345A>C p.T449P Substitution - Missense 15:59058529-59058529 + TCGA-B5-A0JY-01 COSM963407 c.2403G>A p.Q801Q Substitution - coding silent 15:59084234-59084234 + TCGA-AN-A046-01 COSM3816449 c.711G>T p.K237N Substitution - Missense 15:59031533-59031533 + PT13 COSM5896262 c.2090C>T p.S697F Substitution - Missense 15:59081077-59081077 + TCGA-D1-A17Q-01 COSM963383 c.795C>A p.S265S Substitution - coding silent 15:59031617-59031617 + ESO-224 COSM192653 c.2860C>T p.H954Y Substitution - Missense 15:59094799-59094799 + TCGA-AM-5821-01 COSM3754379 c.1701G>A p.V567V Substitution - coding silent 15:59075968-59075968 + NCI-H460 COSM1683204 c.1322delC p.S441fs*1 Deletion - Frameshift 15:59058506-59058506 + T407 COSM4721924 c.683delA p.E230fs*4 Deletion - Frameshift 15:59031505-59031505 + I2L-P19Tb-Tumor-Biopsy COSM2219645 c.1908G>A p.Q636Q Substitution - coding silent 15:59076175-59076175 + TCGA-BS-A0UF-01 COSM963409 c.2512C>T p.R838* Substitution - Nonsense 15:59085747-59085747 + LUAD-NYU315 COSM373578 c.1871G>T p.S624I Substitution - Missense 15:59076138-59076138 + HCC127T COSM3706651 c.2740-5C>A p.? Unknown 15:59092532-59092532 + TCGA-A4-A5Y1-01 COSM3988024 c.981G>T p.E327D Substitution - Missense 15:59052405-59052405 + PCSI_0083_Pa_P COSM2219621 c.1326T>C p.A442A Substitution - coding silent 15:59058510-59058510 + S00829 COSM5659948 c.1520A>T p.Q507L Substitution - Missense 15:59066917-59066917 + YUTUCO COSM3502791 c.2605G>C p.G869R Substitution - Missense 15:59089721-59089721 + TCGA-UC-A7PF-01 COSM4830458 c.910G>C p.E304Q Substitution - Missense 15:59052334-59052334 + 587376 COSM1223884 c.790G>T p.E264* Substitution - Nonsense 15:59031612-59031612 + TCGA-AP-A051-01 COSM963397 c.1487C>T p.A496V Substitution - Missense 15:59066884-59066884 + STC291 COSM192653 c.2860C>T p.H954Y Substitution - Missense 15:59094799-59094799 + LUAD-E00897 COSM364382 c.1868C>T p.S623L Substitution - Missense 15:59076135-59076135 + TCGA-A8-A0A6-01 COSM3816453 c.1288A>C p.T430P Substitution - Missense 15:59058472-59058472 + TCGA-A8-A09Z-01 COSM5202370 c.2809_2812delTGTT p.S939fs*2 Deletion - Frameshift 15:59092606-59092609 + YULAN COSM1708236 c.2072C>T p.A691V Substitution - Missense 15:59081059-59081059 + CSCC-4-T COSM4537804 c.2437G>T p.E813* Substitution - Nonsense 15:59085672-59085672 + TCGA-32-2634-01 COSM3401850 c.128T>C p.I43T Substitution - Missense 15:59030950-59030950 + TCGA-FW-A3R5-06 COSM3887263 c.874C>T p.P292S Substitution - Missense 15:59031696-59031696 + CHC218T COSM4801018 c.1068A>T p.A356A Substitution - coding silent 15:59055742-59055742 + 14T COSM1373799 c.2313delC p.P773fs*44 Deletion - Frameshift 15:59084144-59084144 + TCGA-BR-4184-01 COSM4055913 c.578C>T p.S193L Substitution - Missense 15:59031400-59031400 + 587234 COSM1223882 c.2864T>G p.L955R Substitution - Missense 15:59094803-59094803 + C086 COSM5538282 c.1611C>T p.C537C Substitution - coding silent 15:59067008-59067008 + T2197 COSM4721926 c.1545_1546insCAC p.H520_T521insH Insertion - In frame 15:59066942-59066943 + PET052T COSM5824953 c.1186C>A p.P396T Substitution - Missense 15:59058370-59058370 + 544 COSM5612571 c.2403G>T p.Q801H Substitution - Missense 15:59084234-59084234 + TCGA-EK-A2RK-01 COSM4828950 c.2160C>G p.I720M Substitution - Missense 15:59081147-59081147 + S02376 COSM5696942 c.2224G>T p.A742S Substitution - Missense 15:59081211-59081211 + TCGA-23-1022-01 COSM76256 c.2744A>T p.K915I Substitution - Missense 15:59092541-59092541 + STC291 COSM4721932 c.1881G>A p.A627A Substitution - coding silent 15:59076148-59076148 + TCGA-EI-6917-01 COSM3420480 c.698T>G p.L233* Substitution - Nonsense 15:59031520-59031520 + TCGA-60-2724-01 COSM700836 c.2488T>C p.L830L Substitution - coding silent 15:59085723-59085723 + HCC115T COSM1608520 c.565A>G p.T189A Substitution - Missense 15:59031387-59031387 + TCGA-IR-A3LK-01 COSM4817425 c.2960G>C p.*987S Nonstop extension 15:59094899-59094899 + GB11 COSM1744275 c.1088G>A p.R363Q Substitution - Missense 15:59055762-59055762 + HN_62426 COSM126911 c.2164C>T p.Q722* Substitution - Nonsense 15:59081151-59081151 + TCGA-AA-3715-01 COSM270046 c.246G>A p.Q82Q Substitution - coding silent 15:59031068-59031068 + LUAD-YKER9 COSM351994 c.2672G>C p.G891A Substitution - Missense 15:59091087-59091087 + I2L-P19Tb-Tumor-Biopsy COSM1640306 c.2734delA p.K913fs*29 Deletion - Frameshift 15:59091149-59091149 + TCGA-22-5473-01 COSM700846 c.121G>C p.E41Q Substitution - Missense 15:59030943-59030943 + 477 COSM4438678 c.267C>T p.L89L Substitution - coding silent 15:59031089-59031089 + TCGA-BR-8589-01 COSM4055921 c.1983T>C p.A661A Substitution - coding silent 15:59080970-59080970 + TCGA-B5-A0JY-01 COSM963387 c.948A>C p.E316D Substitution - Missense 15:59052372-59052372 + TCGA-AN-A046-01 COSM1373791 c.1793G>A p.R598Q Substitution - Missense 15:59076060-59076060 + TCGA-BR-8680-01 COSM2219617 c.1094G>A p.R365H Substitution - Missense 15:59055768-59055768 + TCGA-BP-5199-01 COSM470886 c.284G>A p.R95H Substitution - Missense 15:59031106-59031106 + CHEWS001 COSM4578374 c.1987G>C p.A663P Substitution - Missense 15:59080974-59080974 + TCGA-18-3415-01 COSM700844 c.189A>C p.E63D Substitution - Missense 15:59031011-59031011 + SMS-CTR COSM4989584 c.1875G>T p.M625I Substitution - Missense 15:59076142-59076142 + SCMC_RM2_ COSM2219625 c.1456C>A p.P486T Substitution - Missense 15:59066853-59066853 + Pat_15_B COSM5849453 c.1462G>A p.G488R Substitution - Missense 15:59066859-59066859 + PCSI_0083_Pa_X COSM2219621 c.1326T>C p.A442A Substitution - coding silent 15:59058510-59058510 + EOPC-03_tumor COSM3716458 c.703C>T p.Q235* Substitution - Nonsense 15:59031525-59031525 + pfg129T COSM4756157 c.731G>A p.R244Q Substitution - Missense 15:59031553-59031553 + Pat_16_A COSM5849455 c.1546_1548delCAC p.H520delH Deletion - In frame 15:59066943-59066945 + TCGA-LQ-A4E4-01 COSM3816455 c.2297+1G>A p.? Unknown 15:59081285-59081285 + CHC322T COSM3754377 c.27C>G p.N9K Substitution - Missense 15:59030849-59030849 + Pat_01_B COSM5849455 c.1546_1548delCAC p.H520delH Deletion - In frame 15:59066943-59066945 + 24 COSM4778142 c.577T>C p.S193P Substitution - Missense 15:59031399-59031399 + BD124T COSM5493290 c.378T>C p.S126S Substitution - coding silent 15:59031200-59031200 + YUFIT COSM5383609 c.2612C>T p.S871L Substitution - Missense 15:59089728-59089728 + TCGA-BR-4280-01 COSM4055915 c.1416T>C p.P472P Substitution - coding silent 15:59066813-59066813 + Pat_46_A COSM5849451 c.422C>T p.P141L Substitution - Missense 15:59031244-59031244 + Pat_53_A COSM5849455 c.1546_1548delCAC p.H520delH Deletion - In frame 15:59066943-59066945 + TCGA-20-0991-01 COSM72451 c.2712A>T p.R904S Substitution - Missense 15:59091127-59091127 + J76_T COSM3956783 c.1959G>C p.L653F Substitution - Missense 15:59080946-59080946 + SB_06 COSM192642 c.1545T>C p.H515H Substitution - coding silent 15:59066942-59066942 + LIM1215 COSM1373799 c.2313delC p.P773fs*44 Deletion - Frameshift 15:59084144-59084144 + TCGA-AP-A056-01 COSM963385 c.837T>C p.V279V Substitution - coding silent 15:59031659-59031659 + PA285 COSM1163090 c.617C>T p.S206L Substitution - Missense 15:59031439-59031439 + ODG11 COSM5731461 c.1792C>A p.R598R Substitution - coding silent 15:59076059-59076059 + TCGA-UB-A7MB-01 COSM4932387 c.2078A>G p.H693R Substitution - Missense 15:59081065-59081065 + TCGA-AO-A0J3-01 COSM434091 c.1911_1914delCTCT p.L639fs*14 Deletion - Frameshift 15:59076178-59076181 + RK308_C01 COSM3744681 c.1739G>A p.G580D Substitution - Missense 15:59076006-59076006 + TCGA-EE-A3AH-06 COSM3502785 c.1557C>T p.H519H Substitution - coding silent 15:59066954-59066954 + pfg130T COSM4756155 c.536C>T p.A179V Substitution - Missense 15:59031358-59031358 + pfg016T COSM963409 c.2512C>T p.R838* Substitution - Nonsense 15:59085747-59085747 + pfg016T COSM1640304 c.2300G>A p.R767Q Substitution - Missense 15:59084131-59084131 + HCC115 COSM1608520 c.565A>G p.T189A Substitution - Missense 15:59031387-59031387 + TCGA-CM-5861-01 COSM1373789 c.683_684delAA p.K229fs*23 Deletion - Frameshift 15:59031505-59031506 + pfg043T COSM4756161 c.2882T>G p.V961G Substitution - Missense 15:59094821-59094821 + ACINAR03 COSM1373799 c.2313delC p.P773fs*44 Deletion - Frameshift 15:59084144-59084144 + CHC218T COSM4801018 c.1068A>T p.A356A Substitution - coding silent 15:59055742-59055742 + 8015299 COSM3769621 c.2581C>T p.R861C Substitution - Missense 15:59089697-59089697 + T3024 COSM4721928 c.1548C>T p.H516H Substitution - coding silent 15:59066945-59066945 + C086 COSM5538278 c.2128C>T p.P710S Substitution - Missense 15:59081115-59081115 + TCGA-DA-A1I4-06 COSM3502791 c.2605G>C p.G869R Substitution - Missense 15:59089721-59089721 + HT115 COSM2219597 c.568G>T p.E190* Substitution - Nonsense 15:59031390-59031390 + TCGA-DR-A0ZM-01 COSM458991 c.772G>A p.E258K Substitution - Missense 15:59031594-59031594 + TCGA-AX-A0J1-01 COSM963405 c.2187G>T p.Q729H Substitution - Missense 15:59081174-59081174 + AML12 COSM166778 c.1813C>T p.Q605* Substitution - Nonsense 15:59076080-59076080 + TCGA-BS-A0UV-01 COSM963377 c.478G>T p.E160* Substitution - Nonsense 15:59031300-59031300 + YULAD COSM963395 c.1352G>A p.G451D Substitution - Missense 15:59058536-59058536 + I2L-P19Tb-Tumor-Organoid COSM1640306 c.2734delA p.K913fs*29 Deletion - Frameshift 15:59091149-59091149 + C086 COSM5538280 c.2518C>T p.H840Y Substitution - Missense 15:59085753-59085753 + 66 COSM5743694 c.1087C>T p.R363W Substitution - Missense 15:59055761-59055761 + LP6007594 COSM1373791 c.1793G>A p.R598Q Substitution - Missense 15:59076060-59076060 + TCGA-AX-A0J1-01 COSM963391 c.1008G>A p.R336R Substitution - coding silent 15:59055682-59055682 + D-10 COSM4766233 c.883A>G p.S295G Substitution - Missense 15:59052307-59052307 + ESO-D76 COSM1264337 c.1849T>C p.S617P Substitution - Missense 15:59076116-59076116 + TCGA-EE-A3AE-06 COSM3502793 c.2653C>T p.H885Y Substitution - Missense 15:59091068-59091068 + TCGA-DK-A2I4-01 COSM3794273 c.1373C>G p.S458* Substitution - Nonsense 15:59066770-59066770 + TCGA-A5-A0VP-01 COSM963403 c.2033C>T p.P678L Substitution - Missense 15:59081020-59081020 + TCGA-AG-3892-01 COSM257900 c.1165G>T p.E389* Substitution - Nonsense 15:59055839-59055839 + TCGA-A6-6780-01 COSM1373799 c.2313delC p.P773fs*44 Deletion - Frameshift 15:59084144-59084144 + T3174 COSM4252720 c.2056C>T p.P686S Substitution - Missense 15:59081043-59081043 + STC232 COSM5054377 c.1599T>C p.S533S Substitution - coding silent 15:59066996-59066996 + TCGA-29-1702-01 COSM1323920 c.2845C>T p.R949C Substitution - Missense 15:59094784-59094784 + TCGA-EB-A41B-01 COSM3502783 c.730C>T p.R244* Substitution - Nonsense 15:59031552-59031552 + TCGA-EE-A29D-06 COSM3502787 c.2047T>C p.Y683H Substitution - Missense 15:59081034-59081034 + TCGA-G2-A2EF-01 COSM1301269 c.1358C>G p.S453C Substitution - Missense 15:59058542-59058542 + PT33 COSM5909450 c.1687-4C>T p.? Unknown 15:59075950-59075950 + CSCC-45-T COSM4565677 c.238_239GG>AA p.G80N Substitution - Missense 15:59031060-59031061 + sysucc-1163T COSM5458512 c.715C>T p.R239* Substitution - Nonsense 15:59031537-59031537 + CT-TC COSM4989584 c.1875G>T p.M625I Substitution - Missense 15:59076142-59076142 + STC291 COSM5054379 c.2563G>A p.A855T Substitution - Missense 15:59089679-59089679 + PT51 COSM5938365 c.148C>T p.P50S Substitution - Missense 15:59030970-59030970 + TCGA-AA-3852-01 COSM295676 c.1792C>T p.R598* Substitution - Nonsense 15:59076059-59076059 + TCGA-BP-4167-01 COSM1135683 c.1575T>A p.A525A Substitution - coding silent 15:59066972-59066972 + CHEWS027 COSM2219627 c.1575T>C p.A525A Substitution - coding silent 15:59066972-59066972 + TCGA-AZ-4315-01 COSM1373801 c.2683C>T p.R895C Substitution - Missense 15:59091098-59091098 + SNUH_G39_S1 COSM3678232 c.1345A>C p.T449P Substitution - Missense 15:59058529-59058529 + TCGA-D7-A4YU-01 COSM4055923 c.2582G>A p.R861H Substitution - Missense 15:59089698-59089698 + B59-3 COSM1749240 c.2687G>A p.G896E Substitution - Missense 15:59091102-59091102 + Pat_46_B COSM5849451 c.422C>T p.P141L Substitution - Missense 15:59031244-59031244 + PT21_1 COSM5900931 c.1747C>T p.H583Y Substitution - Missense 15:59076014-59076014 + B52 COSM1749238 c.2424G>C p.W808C Substitution - Missense 15:59085659-59085659 + TCGA-22-1016-01 COSM700842 c.881-1G>A p.? Unknown 15:59052304-59052304 + CSCC-44-T COSM555381 c.214C>G p.Q72E Substitution - Missense 15:59031036-59031036 + TCGA-BS-A0UF-01 COSM963381 c.655A>C p.N219H Substitution - Missense 15:59031477-59031477 + TCGA-E9-A3HO-01 COSM3816457 c.2468C>T p.P823L Substitution - Missense 15:59085703-59085703 + TCGA-FW-A3R5-06 COSM3887267 c.2110C>T p.P704S Substitution - Missense 15:59081097-59081097 + TCGA-AB-2905-03 COSM166778 c.1813C>T p.Q605* Substitution - Nonsense 15:59076080-59076080 + Pat_01_B COSM470888 c.2311C>T p.R771C Substitution - Missense 15:59084142-59084142 + TCGA-G2-A2EF-01 COSM1301267 c.1322C>T p.S441L Substitution - Missense 15:59058506-59058506 + BD6T COSM1744275 c.1088G>A p.R363Q Substitution - Missense 15:59055762-59055762 + SNUH_G37_S1 COSM3678234 c.1358C>T p.S453F Substitution - Missense 15:59058542-59058542 + TCGA-B5-A11J-01 COSM963395 c.1352G>A p.G451D Substitution - Missense 15:59058536-59058536 + T3724 COSM4721934 c.2297+2T>C p.? Unknown 15:59081286-59081286 + TCGA-AX-A063-01 COSM434091 c.1911_1914delCTCT p.L639fs*14 Deletion - Frameshift 15:59076178-59076181 + LUAD_E01147 COSM390497 c.1835G>A p.S612N Substitution - Missense 15:59076102-59076102 + SNUH_G17_S1 COSM3678230 c.1327A>C p.T443P Substitution - Missense 15:59058511-59058511 + C135 COSM1264333 c.2034G>A p.P678P Substitution - coding silent 15:59081021-59081021 + EGC15 COSM5054375 c.596G>T p.R199I Substitution - Missense 15:59031418-59031418 + ESO-1154 COSM1264333 c.2034G>A p.P678P Substitution - coding silent 15:59081021-59081021 + TCGA-BR-4280-01 COSM4055919 c.1960A>G p.T654A Substitution - Missense 15:59080947-59080947 + TCGA-BR-6566-01 COSM4055917 c.1801A>G p.I601V Substitution - Missense 15:59076068-59076068 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.404323;Hs.404330;Hs.404331;Hs.404342;Hs.404423 15q21 605840

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.E63D c.189A>C 15 59323210 LUSC A - Frameshift p.K913Rfs*29 c.2738delA 15 59383348 STAD A G Missense p.T13A c.37A>G 15 59323058 LUAD A G Missense p.T654A c.1960A>G 15 59373146 STAD A G Synonymous p.A818A c.2454A>G 15 59377888 LUAD A - IntronicDeletion . c.1367-145delA 15 59358809 ESCA A T IntronicSNV . c.2298-29A>T 15 59376299 SCLC A T Missense p.K915I c.2744A>T 15 59384740 OV A T Missense p.R904S c.2712A>T 15 59383326 OV C - Frameshift p.P773Hfs*44 c.2318delC 15 59376343 STAD C G Missense p.Q680E c.2038C>G 15 59373224 LUSC C G Missense p.Q72E c.214C>G 15 59323235 LUAD C G Missense p.S453C c.1358C>G 15 59350741 BLCA C G Nonsense p.S458* c.1373C>G 15 59358969 BLCA CTCT - Frameshift p.L639Hfs*14 c.1916_1919delTCTC 15 59368377 BRCA CTCT - Frameshift p.L639Hfs*14 c.1916_1919delTCTC 15 59368377 UCEC C T Missense p.H511Y c.1531C>T 15 59359127 UCEC C T Missense p.H885Y c.2653C>T 15 59383267 CM C T Missense p.H954Y c.2860C>T 15 59386998 ESCA C T Missense p.L11F c.31C>T 15 59323052 CM C T Missense p.P678L c.2033C>T 15 59373219 UCEC C T Missense p.P747S c.2239C>T 15 59373425 HNSC C T Missense p.S423F c.1268C>T 15 59350651 BLCA C T Missense p.S441L c.1322C>T 15 59350705 BLCA C T Nonsense p.Q421* c.1261C>T 15 59350644 HNSC C T Nonsense p.Q605* c.1813C>T 15 59368279 AML C T Nonsense p.Q722* c.2164C>T 15 59373350 HNSC C T Nonsense p.R598* c.1792C>T 15 59368258 COREAD C T Nonsense p.R598* c.1792C>T 15 59368258 ESCA C T Nonsense p.R838* c.2512C>T 15 59377946 STAD C T Synonymous p.H519H c.1557C>T 15 59359153 CM C T Synonymous p.L11L c.33C>T 15 59323054 CM G A IntronicSNV . c.1366+18G>A 15 59350767 CM G A Missense p.E298K c.892G>A 15 59344515 BLCA G A Missense p.G35E c.104G>A 15 59323125 CM G A Missense p.G451D c.1352G>A 15 59350735 UCEC G A Missense p.R767Q c.2300G>A 15 59376330 STAD G A SpliceAcceptorSNV . c.881-1G>A 15 59344503 LUSC G A Synonymous p.R767R c.2301G>A 15 59376331 CM GCAATAGTACCACTG - InFrameDeletion p.N447_G451delNSTTG c.1340_1354delATAGTACCACTGGCA 15 59350720 BRCA G C Missense p.E41Q c.121G>C 15 59323142 LUSC G C Missense p.G869R c.2605G>C 15 59381920 CM T A Missense p.I43N c.128T>A 15 59323149 BRCA T C 3-UTRSNV . c.2958+46T>C 15 59387142 CLL T C Missense p.I43T c.128T>C 15 59323149 GBM T C Missense p.I902T c.2705T>C 15 59383319 BRCA T C Missense p.S617P c.1849T>C 15 59368315 ESCA T C Missense p.V395A c.1184T>C 15 59350567 COREAD T C SpliceDonorSNV . c.1007+2T>C 15 59344632 UCEC T C Synonymous p.L830L c.2488T>C 15 59377922 LUSC T C Synonymous p.P472P c.1416T>C 15 59359012 STAD